EP4063366A1 - Kristallform des nukleoproteininhibitors und verwendung davon - Google Patents

Kristallform des nukleoproteininhibitors und verwendung davon Download PDF

Info

Publication number
EP4063366A1
EP4063366A1 EP20890696.6A EP20890696A EP4063366A1 EP 4063366 A1 EP4063366 A1 EP 4063366A1 EP 20890696 A EP20890696 A EP 20890696A EP 4063366 A1 EP4063366 A1 EP 4063366A1
Authority
EP
European Patent Office
Prior art keywords
crystal form
following
ray powder
powder diffraction
diffraction pattern
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP20890696.6A
Other languages
English (en)
French (fr)
Other versions
EP4063366A4 (de
Inventor
Haiying He
Jianhua XIA
Haizhong TAN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chia Tai Tianqing Pharmaceutical Group Co Ltd
Original Assignee
Chia Tai Tianqing Pharmaceutical Group Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chia Tai Tianqing Pharmaceutical Group Co Ltd filed Critical Chia Tai Tianqing Pharmaceutical Group Co Ltd
Publication of EP4063366A1 publication Critical patent/EP4063366A1/de
Publication of EP4063366A4 publication Critical patent/EP4063366A4/de
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/20—Antivirals for DNA viruses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Definitions

  • the present application relates to a crystal form of a nucleoprotein inhibitor and use thereof for preparing a medicament for treating HBV (hepatitis B virus) related diseases.
  • HBV hepatitis B virus
  • Hepatitis B is an inflammatory reaction caused by the invasion of hepatitis B virus, is easy to develop into hepatic fibrosis and cirrhosis, and is a direct cause of 80% of primary liver cancers worldwide.
  • Hepatitis B is a global health problem.
  • Nucleosides and interferons occupy the dominant position in the global anti-hepatitis B drug market, and they are major first-line drugs for treating hepatitis B.
  • disadvantages of high cost, easy relapse and the like Thus, there is a need to develop a novel anti-hepatitis B drug.
  • the present application provides a crystal form of a compound of formula (I), a hydrate thereof, a solvate thereof, or a combination of the hydrate and the solvate
  • the present application provides a crystal form A of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction (XRPD) pattern thereof at the following 2 ⁇ : 6.20 ⁇ 0.20°, 8.90 ⁇ 0.20°, 16.30 ⁇ 0.20° and 24.78 ⁇ 0.20°.
  • XRPD X-ray powder diffraction
  • the aforementioned crystal form A has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.20 ⁇ 0.20°, 8.90 ⁇ 0.20°, 14.22 ⁇ 0.20°, 16.30 ⁇ 0.20°, 22.32 ⁇ 0.20° and 24.78 ⁇ 0.20°.
  • the aforementioned crystal form A has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.20 ⁇ 0.20°, 8.90 ⁇ 0.20°, 11.26 ⁇ 0.20°, 14.22 ⁇ 0.20°, 16.30 ⁇ 0.20°, 17.89 ⁇ 0.20°, 22.32 ⁇ 0.20° and 24.78 ⁇ 0.20°.
  • the aforementioned crystal form A has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.20 ⁇ 0.20°, 8.90 ⁇ 0.20°, 10.09 ⁇ 0.20°, 11.26 ⁇ 0.20°, 14.22 ⁇ 0.20°, 16.30 ⁇ 0.20°, 17.89 ⁇ 0.20°, 20.35 ⁇ 0.20°, 22.32 ⁇ 0.20°, 24.78 ⁇ 0.20° and 27.78 ⁇ 0.20°.
  • the aforementioned crystal form A has an XRPD pattern as shown in FIG. 1 .
  • the aforementioned crystal form A has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 1.
  • Table 1. XRPD pattern data for crystal form A No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 6.20 100.00 8 17.89 10.83 2 8.90 21.04 9 20.35 8.23 3 10.09 8.08 10 22.32 32.65 4 11.26 17.34 11 24.78 37.82 5 11.63 8.91 12 27.78 7.17 6 14.22 18.82 13 28.58 6.05 7 16.30 22.65
  • the aforementioned crystal form A shows a weight loss of 2.50% in a thermogravimetric analysis (TGA) curve upon heating to 200.0 ⁇ 3 °C.
  • TGA thermogravimetric analysis
  • the aforementioned crystal form A has a TGA pattern as shown in FIG. 2 .
  • the aforementioned crystal form A has an endothermic peak in a differential scanning calorimetry (DSC) curve at 234.8 ⁇ 3 °C.
  • the aforementioned crystal form A has a DSC pattern as shown in FIG. 3 .
  • the present application provides a preparation method for the aforementioned crystal form A, which comprises: 1) adding a compound of formula (I) or a crude product thereof to methyl tert -butyl ether; 2) optionally concentrating; and 3) lyophilizing to give the crystal form A.
  • the present application provides a crystal form B of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 9.13 ⁇ 0.20°, 10.53 ⁇ 0.20°, 21.17 ⁇ 0.20° and 22.64 ⁇ 020°.
  • the aforementioned crystal form B has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.13 ⁇ 0.20°, 10.53 ⁇ 0.20°, 11.67 ⁇ 0.20°, 20.09 ⁇ 0.20°, 21.17 ⁇ 0.20° and 22.64 ⁇ 0.20°.
  • the aforementioned crystal form B has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.13 ⁇ 0.20°, 10.53 ⁇ 0.20°, 11.67 ⁇ 0.20°, 13.52 ⁇ 0.20°, 20.09 ⁇ 0.20°, 21.17 ⁇ 0.20° and 22.64 ⁇ 0.20°.
  • the aforementioned crystal form B has an XRPD pattern as shown in FIG. 4 .
  • the aforementioned crystal form B has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 2.
  • Table 2. XRPD pattern data for crystal form B No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 9.13 100.00 2 10.53 48.53 3 11.67 26.24 4 13.52 11.69 5 20.09 20.70 6 21.17 43.87 7 22.64 83.94
  • the aforementioned crystal form B shows a weight loss of 14.37% in a thermogravimetric analysis curve upon heating to 160.0 ⁇ 3 °C.
  • the aforementioned crystal form B has a TGA pattern as shown in FIG. 5 .
  • the aforementioned crystal form B has an endothermic peak in a differential scanning calorimetry (DSC) curve at 149.2 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form B has an endothermic peak in a differential scanning calorimetry (DSC) curve at 236.6 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form B has an endothermic peak in a differential scanning calorimetry (DSC) curve at 149.2 ⁇ 3 °C and/or 236.6 ⁇ 3 °C.
  • the aforementioned crystal form B has a DSC pattern as shown in FIG. 6 .
  • the aforementioned crystal form B is a crystal form of a DMSO solvate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to DMSO in the crystal form B is selected from 1:0.8 to 1:2.0, and preferably 1:1.8.
  • the present application provides a preparation method for the aforementioned crystal form B, which comprises: 1) dissolving a compound of formula (I) in DMSO; and 2) adding water and precipitating a solid to give the crystal form B.
  • the crystal form B is prepared by adding the crystal form A of the compound of formula (I) to DMSO.
  • water is added dropwise in step 2).
  • the present application provides a crystal form C of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 8.94 ⁇ 0.20°, 9.83 ⁇ 0.20° and 10.99 ⁇ 0.20°.
  • the aforementioned crystal form C has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 8.94 ⁇ 0.20°, 9.83 ⁇ 0.20°, 10.99 ⁇ 0.20°, 18.62 ⁇ 0.20° and 19.82 ⁇ 0.20°.
  • the crystal form C has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 8.94 ⁇ 0.20°, 9.83 ⁇ 0.20°, 10.99 ⁇ 0.20°, 13.36 ⁇ 0.20°, 17.21 ⁇ 0.20°, 18.62 ⁇ 0.20°, 19.82 ⁇ 0.20° and 21.56 ⁇ 0.20°.
  • the aforementioned crystal form C has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 8.94 ⁇ 0.20°, 9.39 ⁇ 0.20°, 9.83 ⁇ 0.20°, 10.48 ⁇ 0.20° ⁇ 020°, 10.99 ⁇ 0.20°, 13.36 ⁇ 0.20°, 14.29 ⁇ 0.20°, 17.21 ⁇ 0.20°, 18.14 ⁇ 0.20°, 18.62 ⁇ 0.20°, 19.82 ⁇ 0.20° and 21.56 ⁇ 020°.
  • the aforementioned crystal form C has an XRPD pattern as shown in FIG. 7 .
  • the aforementioned crystal form C has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 3.
  • Table 3. XRPD pattern data for crystal form C No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 8.94 100.00 8 14.29 5.06 2 9.39 19.49 9 17.21 5.84 3 9.83 70.18 10 17.57 4.60 4 10.48 6.90 11 18.14 5.12 5 10.99 28.01 12 18.62 23.44 6 11.75 3.72 13 19.82 20.77 7 13.36 5.77 14 21.56 10.86
  • the aforementioned crystal form C shows a weight loss of 18.33% in a thermogravimetric analysis curve upon heating to 140.0 ⁇ 3 °C.
  • the aforementioned crystal form C has a TGA pattern as shown in FIG. 8 .
  • the aforementioned crystal form C has an endothermic peak in a differential scanning calorimetry (DSC) curve at 103.4 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form C has an endothermic peak in a differential scanning calorimetry (DSC) curve at 236.7 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form C has an exothermic peak in a differential scanning calorimetry (DSC) curve at 218.4 ⁇ 3 °C.
  • the aforementioned crystal form C has an endothermic peak in a differential scanning calorimetry (DSC) curve at 103.4 ⁇ 3 °C and/or 236.7 ⁇ 3 °C, and/or has an exothermic peak at 218.4 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form C has a DSC pattern as shown in FIG. 9 .
  • the aforementioned crystal form C is a crystal form of a hydrate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to water in the crystal form C is selected from 1:6 to 1:8, and preferably 1:6.9.
  • the present application provides a preparation method for the aforementioned crystal form C, which comprises: 1) dissolving a compound of formula (I) in THF; 2) adding MTBE; and 3) precipitating a solid to give the crystal form C.
  • the crystal form C is prepared by adding the crystal form A of the compound of formula (I) to THF.
  • MTBE is added dropwise in step 2).
  • the present application provides a crystal form D of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.52 ⁇ 0.20°, 11.21 ⁇ 0.20°, 12.40 ⁇ 0.20° and 14.41 ⁇ 020°.
  • the crystal form D has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.52 ⁇ 0.20°, 8.70 ⁇ 0.20°, 11.21 ⁇ 0.20°, 12.40 ⁇ 0.20°, 14.41 ⁇ 0.20°, 17.49 ⁇ 0.20° and 22.92 ⁇ 020°.
  • the crystal form D has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.52 ⁇ 0.20°, 8.70 ⁇ 0.20°, 11.21 ⁇ 0.20°, 12.40 ⁇ 0.20°, 14.41 ⁇ 0.20°, 16.06 ⁇ 0.20°, 17.49 ⁇ 020°, 20.98 ⁇ 0.20°, 21.98 ⁇ 0.20° and 22.92 ⁇ 0.20°.
  • the crystal form D has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.17 ⁇ 0.20°, 7.52 ⁇ 0.20°, 7.99 ⁇ 0.20°, 8.70 ⁇ 0.20°, 9.99 ⁇ 0.20°, 10.74 ⁇ 0.20°, 11.21 ⁇ 0.20°, 12.40 ⁇ 0.20°, 14.41 ⁇ 0.20°, 14.88 ⁇ 0.20°, 16.06 ⁇ 0.20°, 17.05 ⁇ 0.20°, 17.49 ⁇ 0.20°, 20.98 ⁇ 0.20°, 21.98 ⁇ 0.20°, 22.48 ⁇ 0.20°, 22.92 ⁇ 0.20°, 23.50 ⁇ 0.20°, 26.47 ⁇ 0.20°, 27.05 ⁇ 0.20° and 28.04 ⁇ 020°.
  • the aforementioned crystal form D has an XRPD pattern as shown in FIG. 10 .
  • the aforementioned crystal form D has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 4. Table 4. XRPD pattern data for crystal form D No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the present application provides a preparation method for the crystal form D, which comprises: 1) dissolving a compound of formula (I) in THF; 2) adding DCM; and 3) precipitating a solid to give the crystal form D.
  • the crystal form D is prepared by adding the crystal form A of the compound of formula (I) to THF.
  • DCM is added dropwise in step 2).
  • the present application provides a crystal form E of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 6.72 ⁇ 020°, 8.53 ⁇ 0.20°, 17.76 ⁇ 020° and 20.38 ⁇ 0.20°.
  • the crystal form E has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.72 ⁇ 0.20°, 8.53 ⁇ 0.20°, 10.50 ⁇ 0.20°, 13.53 ⁇ 0.20°, 17.76 ⁇ 0.20°, 18.83 ⁇ 0.20° and 20.38 ⁇ 020°.
  • the crystal form E has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.72 ⁇ 0.20°, 8.53 ⁇ 0.20°, 10.50 ⁇ 0.20°, 13.53 ⁇ 0.20°, 17.76 ⁇ 0.20°, 18.83 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.06 ⁇ 0.20° and 24.00 ⁇ 0.20°.
  • the crystal form E has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.72 ⁇ 0.20°, 8.53 ⁇ 0.20°, 10.50 ⁇ 0.20°, 11.41 ⁇ 0.20°, 13.53 ⁇ 0.20°, 17.76 ⁇ 0.20°, 18.83 ⁇ 0.20°, 19.99 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.06 ⁇ 0.20°, 22.23 ⁇ 0.20°, 24.00 ⁇ 0.20°, 24.42 ⁇ 0.20° and 25.90 ⁇ 020°.
  • the aforementioned crystal form E has an XRPD pattern as shown in FIG. 11 .
  • the aforementioned crystal form E has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 5.
  • Table 5. XRPD pattern data for crystal form E No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 6.72 22.92 10 19.99 20.73 2 8.53 100.00 11 20.38 29.75 3 10.50 19.66 12 21.06 11.44 4 11.41 11.66 13 22.23 6.20 5 13.53 21.98 14 24.00 14.09 6 14.62 5.42 15 24.42 11.76 7 17.21 5.25 16 25.90 9.97 8 17.76 51.32 17 26.12 5.64 9 18.83 27.17 18 38.27 6.33
  • the aforementioned crystal form E shows a weight loss of 6.61% in a thermogravimetric analysis curve upon heating to 170.0 ⁇ 3 °C, and/or shows a weight loss of 3.53% upon heating from 170 ⁇ 3 °C to 210.0 ⁇ 3 °C.
  • the aforementioned crystal form E has a TGA pattern as shown in FIG. 12 .
  • the aforementioned crystal form E has an endothermic peak in a differential scanning calorimetry (DSC) curve at 236.8 ⁇ 3 °C.
  • the aforementioned crystal form E has a DSC pattern as shown in FIG. 13 .
  • the aforementioned crystal form E is a crystal form of a co-solvate/solvate of 1,4-dioxane and/or water of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I), 1,4-dioxane and water in the crystal form E is selected from 1:0.5-1.0:0.5-1.5, and preferably 1:0.5:1.
  • the present application provides a preparation method for the crystal form E, which comprises: 1) dissolving a compound of formula (I) in 1,4-dioxane; 2) adding acetonitrile to 1,4-dioxane; and 3) precipitating a solid to give the crystal form E.
  • the crystal form E is prepared by adding the crystal form A of the compound of formula (I) to 1,4-dioxane.
  • acetonitrile is added to 1,4-dioxane by evaporating acetonitrile into 1,4-dioxane in step 2).
  • the present application provides a crystal form F of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 4.18 ⁇ 0.20°, 8.35 ⁇ 0.20°, 10.58 ⁇ 0.20° and 16.86 ⁇ 0.20°.
  • the aforementioned crystal form F has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 4.18 ⁇ 0.20°, 8.35 ⁇ 0.20°, 10.58 ⁇ 0.20°, 11.87 ⁇ 0.20°, 16.86 ⁇ 0.20° and 21.16 ⁇ 0.20°.
  • the aforementioned crystal form F has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 4.18 ⁇ 0.20°, 8.35 ⁇ 0.20°, 10.58 ⁇ 0.20°, 11.87 ⁇ 0.20°, 12.32 ⁇ 020°, 16.86 ⁇ 0.20°, 21.16 ⁇ 0.20°, 25.47 ⁇ 0.20° and 29.17 ⁇ 0.20°.
  • the aforementioned crystal form F has an XRPD pattern as shown in FIG. 14 .
  • the aforementioned crystal form F has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 6.
  • Table 6 XRPD pattern data for crystal form F No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 4.18 15.97 6 16.86 100.00 2 8.35 49.02 7 21.16 17.25 3 10.58 16.50 8 25.47 6.85 4 11.87 8.35 9 29.17 7.10 5 12.32 6.29
  • the aforementioned crystal form F shows a weight loss of 3.22% in a thermogravimetric analysis curve upon heating to 150.0 ⁇ 3 °C.
  • the aforementioned crystal form F has a TGA pattern as shown in FIG. 15 .
  • the aforementioned crystal form F has an endothermic peak in a differential scanning calorimetry (DSC) curve at 229.9 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form F has an endothermic peak in a differential scanning calorimetry (DSC) curve at 188.6 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form F has an endothermic peak in a differential scanning calorimetry (DSC) curve at 98.9 ⁇ 3 °C.
  • the aforementioned crystal form F has an endothermic peak in a differential scanning calorimetry (DSC) curve at 229.9 ⁇ 3 °C and/or 188.6 ⁇ 3 °C and/or 98.9 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form F has a DSC pattern as shown in FIG. 16 .
  • the aforementioned crystal form F is a crystal form of a hydrate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to water in the crystal form F is selected from 1:0.8 to 1:1.2, and preferably 1:1.
  • the present application provides a preparation method for the aforementioned crystal form F, which comprises: 1) dissolving a compound of formula (I) in DMF; 2) mixing the resulting solution with water; and 3) precipitating a solid to give the crystal form F.
  • the crystal form F is prepared by adding the crystal form A of the compound of formula (I) to DMF.
  • the means for mixing the solution with water is selected from dropwise addition of the solution to water.
  • the present application provides a crystal form G of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.31 ⁇ 0.20°, 19.18 ⁇ 0.20° and 25.99 ⁇ 0.20°.
  • the crystal form G has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.31 ⁇ 0.20°, 15.86 ⁇ 0.20°, 19.18 ⁇ 0.20°, 21.05 ⁇ 0.20° and 25.99 ⁇ 0.20°.
  • the crystal form G has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.31 ⁇ 0.20°, 11.62 ⁇ 0.20°, 12.91 ⁇ 0.20°, 15.86 ⁇ 0.20°, 19.18 ⁇ 0.20°, 21.05 ⁇ 0.20°, 24.67 ⁇ 0.20° and 25.99 ⁇ 0.20°.
  • the crystal form G has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.31 ⁇ 020°, 11.62 ⁇ 0.20°, 12.91 ⁇ 020°, 15.86 ⁇ 0.20°, 17.17 ⁇ 0.20°, 18.20 ⁇ 0.20°, 19.18 ⁇ 0.20°, 19.74 ⁇ 0.20°, 21.05 ⁇ 0.20°, 21.30 ⁇ 0.20°, 24.67 ⁇ 0.20° and 25.99 ⁇ 0.20°.
  • the aforementioned crystal form G has an XRPD pattern as shown in FIG. 17 .
  • the aforementioned crystal form G has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 7.
  • Table 7. XRPD pattern data for crystal form G No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.03 33.31 8 19.18 39.43 2 8.31 100.00 9 19.76 21.14 3 11.62 13.71 10 21.05 27.73 4 12.91 22.79 11 21.30 16.25 5 15.86 25.81 12 24.67 19.44 6 17.12 8.42 13 25.99 38.36 7 18.20 14.31
  • the aforementioned crystal form G shows a weight loss of 7.39% in a thermogravimetric analysis curve upon heating to 150.0 ⁇ 3 °C.
  • the aforementioned crystal form G has a TGA pattern as shown in FIG. 18 .
  • the aforementioned crystal form G has an endothermic peak in a differential scanning calorimetry (DSC) curve at 235.7 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form G has an exothermic peak in a differential scanning calorimetry (DSC) curve at 177.8 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form G has an endothermic peak in a differential scanning calorimetry (DSC) curve at 235.7 ⁇ 3 °C, and/or has an exothermic peak at 177.8 ⁇ 3 °C.
  • the aforementioned crystal form G has a DSC pattern as shown in FIG. 19 .
  • the present application provides a preparation method for the crystal form G, which comprises: 1) adding a compound of formula (I) to a mixed solvent of CHCl 3 and THF; and 2) precipitating a solid and separating to give the crystal form G.
  • the crystal form A of the compound of formula (I) is added to the mixed solvent of CHCl 3 and THF.
  • the present application provides a crystal form H of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.05 ⁇ 0.20°, 9.10 ⁇ 0.20°, 10.78 ⁇ 0.20° and 22.90 ⁇ 0.20°.
  • the aforementioned crystal form H has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.05 ⁇ 0.20°, 9.10 ⁇ 0.20°, 10.78 ⁇ 0.20°, 21.24 ⁇ 0.20°, 21.74 ⁇ 0.20° and 22.90 ⁇ 020°.
  • the aforementioned crystal form H has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.05 ⁇ 0.20°, 9.10 ⁇ 0.20°, 10.78 ⁇ 0.20°, 13.07 ⁇ 0.20°, 19.57 ⁇ 020°, 21.24 ⁇ 0.20°, 21.74 ⁇ 0.20°, 22.24 ⁇ 0.20° and 22.90 ⁇ 0.20°.
  • the aforementioned crystal form H has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.05 ⁇ 0.20°, 9.10 ⁇ 0.20°, 10.78 ⁇ 0.20°, 11.34 ⁇ 0.20°, 13.07 ⁇ 0.20°, 14.07 ⁇ 020°, 14.99 ⁇ 0.20°, 15.86 ⁇ 0.20°, 16.17 ⁇ 0.20°, 18.60 ⁇ 0.20°, 19.57 ⁇ 0.20°, 21.24 ⁇ 0.20°, 21.46 ⁇ 0.20°, 21.74 ⁇ 0.20°, 2224 ⁇ 0.20°, 22.72 ⁇ 0.20° and 22.90 ⁇ 0.20°.
  • the aforementioned crystal form H has an XRPD pattern as shown in FIG. 20 .
  • the aforementioned crystal form H has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 8.
  • Table 8. XRPD pattern data for crystal form H No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the aforementioned crystal form H shows a weight loss of 11.77% in a thermogravimetric analysis curve upon heating to 160.0 ⁇ 3 °C.
  • the aforementioned crystal form H has a TGA pattern as shown in FIG. 21 .
  • the aforementioned crystal form H has an endothermic peak in a differential scanning calorimetry (DSC) curve at 140.4 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form H has an endothermic peak in a differential scanning calorimetry (DSC) curve at 236.9 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form H has an endothermic peak in a differential scanning calorimetry (DSC) curve at 140.4 ⁇ 3 °C and/or 236.9 ⁇ 3 °C.
  • the aforementioned crystal form H has a DSC pattern as shown in FIG. 22 .
  • the aforementioned crystal form H is a crystal form of a DMF solvate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to DMF in the crystal form H is selected from 1:0.6 to 1:1.0, and preferably 1:0.8.
  • the present application provides a preparation method for the crystal form H, which comprises: 1) adding a compound of formula (I) to a mixed solvent of EtOH and DMF; and 2) precipitating a solid and separating to give the crystal form H.
  • the crystal form H is prepared by adding the crystal form A of the compound of formula (I) to the mixed solvent of EtOH and DMF.
  • the present application provides a crystal form I of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 5.56 ⁇ 0.20°, 11.25 ⁇ 0.20° and 14.09 ⁇ 0.20°.
  • the crystal form I has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 5.56 ⁇ 0.20°, 7.54 ⁇ 0.20°, 11.25 ⁇ 0.20°, 14.09 ⁇ 0.20° and 19.64 ⁇ 0.20°. In some embodiments of the present application, the crystal form I has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 5.56 ⁇ 0.20°, 7.54 ⁇ 0.20°, 11.25 ⁇ 0.20°, 14.09 ⁇ 0.20°, 18.07 ⁇ 0.20°, 19.64 ⁇ 0.20° and 20.33 ⁇ 0.20°.
  • the aforementioned crystal form I has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 5.56 ⁇ 0.20°, 7.54 ⁇ 0.20°, 11.25 ⁇ 0.20°, 14.09 ⁇ 0.20°, 18.07 ⁇ 0.20°, 19.64 ⁇ 0.20°, 20.33 ⁇ 0.20°, 21.65 ⁇ 0.20° and 22.31 ⁇ 020°.
  • the aforementioned crystal form I has an XRPD pattern as shown in FIG. 23 .
  • the aforementioned crystal form I has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 9.
  • Table 9. XRPD pattern data for crystal form I No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 5.56 100.00 7 20.33 8.33 2 7.54 11.90 8 21.65 5.77 3 11.25 16.35 9 22.31 6.69 4 14.09 13.45 10 25.43 4.70 5 18.07 8.01 11 30.23 4.67 6 19.64 8.70
  • the aforementioned crystal form I shows a weight loss of 3.52% in a thermogravimetric analysis curve upon heating to 100.0 ⁇ 3 °C.
  • the aforementioned crystal form I has a TGA pattern as shown in FIG. 24 .
  • the aforementioned crystal form I has an endothermic peak in a differential scanning calorimetry (DSC) curve at 94.7 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form I has an endothermic peak in a differential scanning calorimetry (DSC) curve at 234.4 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form I has an exothermic peak in a differential scanning calorimetry (DSC) curve at 185.2 ⁇ 3 °C.
  • the aforementioned crystal form I has an endothermic peak in a differential scanning calorimetry (DSC) curve at 94.7 ⁇ 3 °C and/or 234.4 ⁇ 3 °C, and/or has an exothermic peak in the DSC curve at 185.2 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form I has a DSC pattern as shown in FIG. 25 .
  • the aforementioned crystal form I is a crystal form of a hydrate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to water in the crystal form I is selected from 1:1.0 to 1:1.2, and preferably 1:1.1.
  • the present application provides a preparation method for the crystal form I, which comprises: 1) adding a compound of formula (I) to water; and 2) suspending, stirring and separating to give the crystal form I.
  • the crystal form I is prepared by adding the crystal form A of the compound of formula (I) to water.
  • stirring is performed under heating.
  • the heating temperature is selected from 45 °C to 60 °C, or is 55 °C.
  • the present application provides a crystal form J of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 9.28 ⁇ 0.20°, 10.34 ⁇ 0.20°, 22.66 ⁇ 0.20° and 26.12 ⁇ 0.20°.
  • the aforementioned crystal form J has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.28 ⁇ 0.20°, 10.34 ⁇ 0.20°, 19.45 ⁇ 0.20°, 20.93 ⁇ 0.20°, 22.66 ⁇ 0.20° and 26.12 ⁇ 0.20°.
  • the aforementioned crystal form J has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.28 ⁇ 0.20°, 10.34 ⁇ 0.20°, 12.35 ⁇ 0.20°, 14.95 ⁇ 0.20°, 17.88 ⁇ 0.20°, 19.45 ⁇ 0.20°, 20.93 ⁇ 0.20°, 22.66 ⁇ 0.20° and 26.12 ⁇ 0.20°.
  • the aforementioned crystal form J has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 3.47 ⁇ 0.20°, 9.28 ⁇ 0.20°, 10.34 ⁇ 0.20°, 10.92 ⁇ 0.20°, 12.35 ⁇ 0.20°, 14.95 ⁇ 0.20°, 17.62 ⁇ 020°, 17.88 ⁇ 0.20°, 19.09 ⁇ 0.20°, 19.45 ⁇ 0.20°, 20.08 ⁇ 0.20°, 20.93 ⁇ 0.20°, 22.66 ⁇ 0.20°, 23.98 ⁇ 0.20°, 26.12 ⁇ 0.20° and 28.63 ⁇ 0.20°.
  • the aforementioned crystal form J has an XRPD pattern as shown in FIG. 26 .
  • the aforementioned crystal form J has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 10.
  • Table 10 XRPD pattern data for crystal form J No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the aforementioned crystal form J shows a weight loss of 27.46% in a thermogravimetric analysis curve upon heating to 140.0 ⁇ 3 °C.
  • the aforementioned crystal form J has a TGA pattern as shown in FIG. 27 .
  • the aforementioned crystal form J has an endothermic peak in a differential scanning calorimetry (DSC) curve at 86.7 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form J has an endothermic peak in a differential scanning calorimetry (DSC) curve at 229.4 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form J has an endothermic peak in a differential scanning calorimetry (DSC) curve at 150.0 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form J has an exothermic peak in a differential scanning calorimetry (DSC) curve at 148.6 ⁇ 3 °C.
  • the aforementioned crystal form J has an endothermic peak in a differential scanning calorimetry (DSC) curve at 86.7 ⁇ 3 °C and/or 150.0 ⁇ 3 °C and/or 229.4 ⁇ 3 °C, and/or has an exothermic peak in the DSC curve at 148.6 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form J has a DSC pattern as shown in FIG. 28 .
  • the present application provides a preparation method for the crystal form J, which comprises: 1) adding the compound of formula (I) to 2-MeTHF; and 2) suspending, stirring and separating to give the crystal form J.
  • the crystal form J is prepared by adding the crystal form A of the compound of formula (I) to 2-MeTHF.
  • stirring is performed under heating; in some embodiments of the present application, the heating temperature is selected from 45 °C to 60 °C, or is 50 °C.
  • the present application provides a crystal form K of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.49 ⁇ 020°, 8.46 ⁇ 0.20°, 15.99 ⁇ 020° and 17.02 ⁇ 0.20°.
  • the aforementioned crystal form K has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.49 ⁇ 0.20°, 8.46 ⁇ 0.20°, 13.18 ⁇ 0.20°, 14.43 ⁇ 0.20°, 15.99 ⁇ 0.20° and 17.02 ⁇ 020°.
  • the aforementioned crystal form K has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.49 ⁇ 0.20°, 8.46 ⁇ 0.20°, 9.91 ⁇ 020°, 13.18 ⁇ 0.20°, 14.43 ⁇ 0.20°, 15.99 ⁇ 0.20°, 17.02 ⁇ 0.20°, 20.97 ⁇ 0.20° and 24.20 ⁇ 0.20°.
  • the aforementioned crystal form K has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.49 ⁇ 0.20°, 8.46 ⁇ 0.20°, 9.12 ⁇ 0.20°, 9.91 ⁇ 0.20°, 10.67 ⁇ 0.20°, 13.18 ⁇ 0.20°, 14.43 ⁇ 0.20°, 15.99 ⁇ 0.20°, 17.02 ⁇ 0.20°, 18.34 ⁇ 0.20°, 19.95 ⁇ 0.20°, 20.29 ⁇ 0.20°, 20.97 ⁇ 0.20°, 21.66 ⁇ 0.20°, 23.03 ⁇ 0.20°, 24.20 ⁇ 0.20°, 24.94 ⁇ 0.20° and 25.69 ⁇ 0.20°.
  • the aforementioned crystal form K has an XRPD pattern as shown in FIG. 29 .
  • the aforementioned crystal form K has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 11. Table 11. XRPD pattern data for crystal form K No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the aforementioned crystal form K shows a weight loss of 1.35% in a thermogravimetric analysis curve upon heating to 150.0 ⁇ 3 °C.
  • the aforementioned crystal form K has a TGA pattern as shown in FIG. 30 .
  • the aforementioned crystal form K has an endothermic peak in a differential scanning calorimetry (DSC) curve at 231.2 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form K has an exothermic peak in a differential scanning calorimetry (DSC) curve at 164.1 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form K has an endothermic peak in a differential scanning calorimetry (DSC) curve at 160.6 ⁇ 3 °C.
  • the aforementioned crystal form K has an endothermic peak in a differential scanning calorimetry (DSC) curve at 231.2 ⁇ 3 °C and/or 160.6 ⁇ 3 °C, and/or has an exothermic peak in the DSC curve at 164.1 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form K has a DSC pattern as shown in FIG. 31 .
  • the present application provides a preparation method for the crystal form K, which comprises: 1) adding the compound of formula (I) to a mixed solvent of DCM and MeOH; and 2) precipitating a solid and separating to give the crystal form K.
  • the crystal form K is prepared by adding the crystal form A of the compound of formula (I) to the mixed solvent of DCM and MeOH.
  • dissolving is performed under heating.
  • the heating temperature is selected from 45 °C to 60 °C, or is 50 °C.
  • the solid in the preparation method for the crystal form K, the solid is precipitated by cooling in step 2).
  • the present application provides a crystal form L of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 8.53 ⁇ 0.20°, 11.09 ⁇ 0.20°, 22.34 ⁇ 0.20° and 23.12 ⁇ 0.20°.
  • the aforementioned crystal form L has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 8.53 ⁇ 0.20°, 11.09 ⁇ 0.20°, 15.00 ⁇ 0.20°, 20.76 ⁇ 0.20°, 22.34 ⁇ 0.20° and 23.12 ⁇ 0.20°.
  • the aforementioned crystal form L has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.53 ⁇ 0.20°, 11.09 ⁇ 0.20°, 14.14 ⁇ 0.20°, 15.00 ⁇ 0.20°, 20.76 ⁇ 0.20°, 22.34 ⁇ 0.20°, 23.12 ⁇ 0.20° and 26.85 ⁇ 0.20°.
  • the aforementioned crystal form L has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.53 ⁇ 0.20°, 10.50 ⁇ 0.20°, 11.09 ⁇ 0.20°, 14.14 ⁇ 0.20°, 15.00 ⁇ 0.20°, 20.76 ⁇ 020°, 22.34 ⁇ 0.20°, 23.12 ⁇ 0.20° and 26.85 ⁇ 0.20°.
  • the aforementioned crystal form L has an XRPD pattern as shown in FIG. 32 .
  • the aforementioned crystal form L has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 12.
  • Table 12. XRPD pattern data for crystal form L No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.03 13.73 9 20.76 35.20 2 7.91 5.21 10 21.30 11.53 3 8.53 76.66 11 21.55 5.15 4 10.50 18.12 12 22.34 49.63 5 11.09 82.87 13 23.12 100.00 6 14.14 11.11 14 25.89 4.63 7 15.00 25.17 15 26.85 22.11 8 20.15 7.41 16 32.16 6.88
  • the aforementioned crystal form L shows a weight loss of 10.37% in a thermogravimetric analysis curve upon heating to 160.0 ⁇ 3 °C.
  • the aforementioned crystal form L has a TGA pattern as shown in FIG. 33 .
  • the aforementioned crystal form L has an endothermic peak in a differential scanning calorimetry (DSC) curve at 150.1 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form L has an endothermic peak in a differential scanning calorimetry (DSC) curve at 210.7 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form L has an endothermic peak in a differential scanning calorimetry (DSC) curve at 150.1 ⁇ 3 °C and/or 210.7 ⁇ 3 °C.
  • the aforementioned crystal form L has a DSC pattern as shown in FIG. 34 .
  • the aforementioned crystal form L is a crystal form of an NMP solvate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to NMP in the crystal form L is selected from 1:0.5 to 1:1.0, and preferably 1:0.8.
  • the present application provides a preparation method for the aforementioned crystal form L, which comprises: 1) dissolving a compound of formula (I) in NMP; 2) adding EtOAc to the resulting NMP solution; and 3) precipitating a solid and separating to give the crystal form L.
  • the crystal form L is prepared by adding the crystal form A of the compound of formula (I) to NMP.
  • EtOAc is added to NMP by evaporating EtOAc into NMP in step 2).
  • the present application provides a crystal form M of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 9.32 ⁇ 0.20°, 10.43 ⁇ 0.20°, 12.46 ⁇ 0.20° and 19.62 ⁇ 0.20°.
  • the aforementioned crystal form M has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.32 ⁇ 0.20°, 10.43 ⁇ 0.20°, 10.81 ⁇ 0.20°, 12.46 ⁇ 0.20°, 19.62 ⁇ 0.20° and 21.03 ⁇ 0.20°.
  • the aforementioned crystal form M has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.32 ⁇ 0.20°, 10.43 ⁇ 0.20°, 10.81 ⁇ 0.20°, 12.46 ⁇ 0.20°, 17.55 ⁇ 0.20°, 17.99 ⁇ 0.20°, 19.62 ⁇ 0.20°, 21.03 ⁇ 0.20° and 22.90 ⁇ 0.20°.
  • the crystal form M has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 9.32 ⁇ 0.20°, 10.43 ⁇ 0.20°, 10.81 ⁇ 0.20°, 12.46 ⁇ 0.20°, 13.00 ⁇ 0.20°, 15.06 ⁇ 0.20°, 17.55 ⁇ 0.20°, 17.99 ⁇ 0.20°, 19.62 ⁇ 0.20°, 21.03 ⁇ 0.20° and 22.90 ⁇ 0.20°.
  • the aforementioned crystal form M has an XRPD pattern as shown in FIG. 35 .
  • the aforementioned crystal form M has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 13.
  • Table 13 XRPD pattern data for crystal form M No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 9.32 100.00 7 17.55 10.37 2 10.43 79.23 8 17.99 6.83 3 10.81 17.00 9 19.62 19.48 4 12.46 20.62 10 21.03 19.15 5 13.00 6.65 11 22.90 14.14 6 15.06 5.75 12 26.43 3.59
  • the aforementioned crystal form M shows a weight loss of 10.98% in a thermogravimetric analysis curve upon heating to 130.0 ⁇ 3 °C.
  • the aforementioned crystal form M has a TGA pattern as shown in FIG. 36 .
  • the aforementioned crystal form M has an endothermic peak in a differential scanning calorimetry (DSC) curve at 109.7 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form M has an endothermic peak in a differential scanning calorimetry (DSC) curve at 235.9 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form M has an endothermic peak in a differential scanning calorimetry (DSC) curve at 109.7 ⁇ 3 °C and/or 235.9 ⁇ 3 °C.
  • the aforementioned crystal form M has a DSC pattern as shown in FIG. 37 .
  • the aforementioned crystal form M is a crystal form of a THF solvate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to TMF in the crystal form M is selected from 1:0.6 to 1:1.0, and preferably 1:0.8.
  • the present application provides a preparation method for the aforementioned crystal form M, which comprises: 1) dissolving a compound of formula (I) in THF; and 2) precipitating a solid and separating to give the crystal form M.
  • the crystal form M is prepared by adding the crystal form A of the compound of formula (I) to THF.
  • the present application provides a crystal form N of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 8.47° ⁇ 0.20°, 12.62 ⁇ 0.20°, 15.70 ⁇ 0.20° and 18.41 ⁇ 0.20°.
  • the aforementioned crystal form N has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 8.47 ⁇ 0.20°, 11.23 ⁇ 0.20°, 12.62 ⁇ 0.20°, 15.70 ⁇ 0.20°, 18.41 ⁇ 0.20° and 21.49 ⁇ 0.20°.
  • the aforementioned crystal form N has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.04 ⁇ 0.20°, 8.47 ⁇ 0.20°, 10.01 ⁇ 0.20°, 11.23 ⁇ 0.20°, 12.62 ⁇ 0.20°, 15.70 ⁇ 0.20°, 18.41 ⁇ 0.20°, 21.49 ⁇ 0.20° and 22.53 ⁇ 0.20°.
  • the aforementioned crystal form N has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.04 ⁇ 0.20°, 8.47 ⁇ 0.20°, 10.01 ⁇ 0.20°, 11.23 ⁇ 0.20°, 12.62 ⁇ 0.20°, 15.70 ⁇ 0.20°, 17.32 ⁇ 020°, 18.41 ⁇ 0.20°, 20.31 ⁇ 0.20°, 21.49 ⁇ 0.20°, 22.53 ⁇ 0.20° and 26.34 ⁇ 0.20°.
  • the aforementioned crystal form N has an XRPD pattern as shown in FIG. 38 .
  • the aforementioned crystal form N has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 14.
  • Table 14. XRPD pattern data for crystal form N No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.04 12.38 8 18.41 100.00 2 8.47 14.77 9 20.31 6.19 3 10.01 16.20 10 21.49 27.42 4 11.23 43.59 11 22.53 20.36 5 12.62 76.09 12 26.34 8.28 6 15.70 69.18 13 30.67 5.98 7 17.32 6.52
  • the aforementioned crystal form N shows a weight loss of 1.99% in a thermogravimetric analysis curve upon heating to 200.0 ⁇ 3 °C.
  • the aforementioned crystal form N has a TGA pattern as shown in FIG. 39 .
  • the aforementioned crystal form N has an endothermic peak in a differential scanning calorimetry (DSC) curve at 236.3 ⁇ 3 °C.
  • the aforementioned crystal form N has a DSC pattern as shown in FIG. 40 .
  • the present application provides a preparation method for the aforementioned crystal form N, which comprises: 1) dissolving a compound of formula (I) in EtOH; and 2) precipitating a solid and separating to give the crystal form N.
  • the crystal form N is prepared by adding the crystal form A of the compound of formula (I) to EtOH.
  • the present application provides a crystal form O of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.50 ⁇ 0.20°, 10.65 ⁇ 0.20° and 11.10 ⁇ 0.20°.
  • the aforementioned crystal form O has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.18 ⁇ 0.20°, 7.50 ⁇ 0.20°, 10.65 ⁇ 0.20°, 11.10 ⁇ 0.20°, 14.04 ⁇ 0.20° and 21.48 ⁇ 0.20°.
  • the aforementioned crystal form O has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.18 ⁇ 0.20°, 7.50 ⁇ 0.20°, 10.65 ⁇ 0.20°, 11.10 ⁇ 0.20°, 14.04 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.79 ⁇ 0.20° and 27.02 ⁇ 0.20°.
  • the crystal form O has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.18 ⁇ 0.20°, 7.50 ⁇ 0.20°, 10.65 ⁇ 0.20°, 11.10 ⁇ 0.20°, 14.04 ⁇ 0.20°, 15.67 ⁇ 0.20°, 19.16 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.79 ⁇ 0.20°, 23.39 ⁇ 0.20°, 26.28 ⁇ 0.20° and 27.02 ⁇ 0.20°.
  • the aforementioned crystal form O has an XRPD pattern as shown in FIG. 41 .
  • the aforementioned crystal form O has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 15.
  • Table 15. XRPD pattern data for crystal form O No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.18 51.90 7 19.16 5.60 2 7.50 100.00 8 21.48 10.95 3 10.65 15.11 9 22.79 8.75 4 11.10 40.78 10 23.39 5.06 5 14.04 9.85 11 26.28 7.39 6 15.67 4.86 12 27.02 9.30
  • the aforementioned crystal form O shows a weight loss of 2.23% in a thermogravimetric analysis curve upon heating to 140.0 ⁇ 3 °C.
  • the aforementioned crystal form O has a TGA pattern as shown in FIG. 42 .
  • the aforementioned crystal form O has an endothermic peak in a differential scanning calorimetry (DSC) curve at 123.3 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form O has an exothermic peak in a differential scanning calorimetry (DSC) curve at 128.5 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form O has an endothermic peak in a differential scanning calorimetry (DSC) curve at 231.1 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form O has an endothermic peak in a differential scanning calorimetry (DSC) curve at 237.1 ⁇ 3 °C.
  • the aforementioned crystal form O has an endothermic peak in a differential scanning calorimetry (DSC) curve at 123.3 ⁇ 3 °C and/or 231.1 ⁇ 3 °C and/or 237.1 ⁇ 3 °C, and/or has an exothermic peak in the DSC curve at 128.5 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form O has a DSC pattern as shown in FIG. 43 .
  • the aforementioned crystal form O is a crystal form of a hydrate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to water in the crystal form O is selected from 1:0.6 to 1:1.0, and preferably 1:0.7.
  • the present application provides a preparation method for the crystal form O, which comprises: drying the aforementioned crystal form D under vacuum at room temperature to give the crystal form O.
  • the present application provides a crystal form P of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.08 ⁇ 0.20° and 21.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 21.25 ⁇ 0.20° and 21.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 26.74 ⁇ 0.20° and 27.46 ⁇ 0.20°. In some embodiments of the present application, the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.48 ⁇ 0.20°, 26.74 ⁇ 0.20° and 27.46 ⁇ 020°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 020°, 12.92 ⁇ 0.20°, 18.61 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 0.20°, 26.74 ⁇ 0.20°, 27.46 ⁇ 0.20° and 27.83 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 12.92 ⁇ 0.20°, 18.61 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 0.20°, 25.01 ⁇ 0.20°, 26.74 ⁇ 0.20°, 27.46 ⁇ 0.20° and 27.83 ⁇ 0.20°.
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 15.36 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20° and 22.71 ⁇ 0.20°. In some embodiments of the present application, the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 020°, 12.92 ⁇ 0.20°, 15.36 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 0.20° and 27.46 ⁇ 020°.
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 12.92 ⁇ 0.20°, 15.36 ⁇ 020°, 20.39 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 020°, 26.74 ⁇ 020° and 27.46 ⁇ 0.20°.
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 020°, 12.92 ⁇ 0.20°, 15.36 ⁇ 0.20°, 18.61 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 0.20°, 26.74 ⁇ 0.20°, 27.46 ⁇ 0.20° and 27.83 ⁇ 0.20°.
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 11.61 ⁇ 0.20°, 12.92 ⁇ 0.20°, 15.36 ⁇ 0.20°, 15.89 ⁇ 0.20°, 18.61 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 0.20°, 26.74 ⁇ 0.20°, 27.46 ⁇ 0.20° and 27.83 ⁇ 0.20°.
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.08 ⁇ 0.20°, 11.61 ⁇ 0.20°, 12.92 ⁇ 0.20°, 15.36 ⁇ 0.20°, 15.89 ⁇ 0.20°, 18.61 ⁇ 0.20°, 19.89 ⁇ 0.20°, 20.39 ⁇ 0.20°, 21.25 ⁇ 0.20°, 21.48 ⁇ 0.20°, 22.71 ⁇ 0.20°, 26.05 ⁇ 0.20°, 26.74 ⁇ 0.20°, 27.46 ⁇ 0.20° and 27.83 ⁇ 0.20°.
  • the aforementioned crystal form P has an XRPD pattern as shown in FIG. 44A or FIG. 44B .
  • the aforementioned crystal form P has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 16A.
  • Table 16A XRPD pattern data for crystal form P No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.08 100.00 14 21.48 27.17 3 12.92 3.83 15 22.71 4.17 4 14.25 2.64 16 25.01 3.17 5 15.36 2.73 18 26.74 6.42 9 18.61 4.23 19 27.46 5.07 12 20.39 5.87 20 27.83 4.86 13 21.25 15.87
  • the aforementioned crystal form P has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 16B.
  • Table 16B XRPD pattern data for crystal form P No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the aforementioned crystal form P shows a weight loss of 2.76% in a thermogravimetric analysis curve upon heating to 150.0 ⁇ 3 °C.
  • the aforementioned crystal form P has a TGA pattern as shown in FIG. 45 .
  • the aforementioned crystal form P has an endothermic peak in a differential scanning calorimetry (DSC) curve at 236.1 ⁇ 3 °C.
  • the aforementioned crystal form P has a DSC pattern as shown in FIG. 46 .
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20° and 21.46 ⁇ 0.20°. In some embodiments of the present application, the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 21.28 ⁇ 0.20° and 21.46 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°. In some embodiments of the present application, the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.46 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 24.84 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 15.40 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20° and 22.74 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 8.74 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 15.92 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 8.74 ⁇ 0.20°, 11.66 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 15.92 ⁇ 0.20°, 16.22 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 8.74 ⁇ 0.20°, 929 ⁇ 0.20°, 11.66 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 15.92 ⁇ 0.20°, 16.22 ⁇ 0.20°, 17.54 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has an XRPD pattern as shown in FIG. 59 .
  • the aforementioned crystal form P has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 16C.
  • Table 16C XRPD pattern data for crystal form P No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the present application provides a crystal form P of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.12 ⁇ 0.20° and 21.46 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 21.28 ⁇ 0.20° and 21.46 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°. In some embodiments of the present application, the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.46 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 24.84 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the present application provides a crystal form P of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.12 ⁇ 0.20°, 15.40 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20° and 22.74 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the present application provides a crystal form P of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.12 ⁇ 0.20°, 8.74 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 15.92 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20° and 27.48 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 8.74 ⁇ 0.20°, 11.66 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 15.92 ⁇ 0.20°, 16.22 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.12 ⁇ 0.20°, 8.74 ⁇ 0.20°, 9.29 ⁇ 0.20°, 11.66 ⁇ 0.20°, 12.96 ⁇ 0.20°, 15.40 ⁇ 0.20°, 15.92 ⁇ 0.20°, 16.22 ⁇ 0.20°, 17.54 ⁇ 0.20°, 18.66 ⁇ 0.20°, 20.38 ⁇ 0.20°, 21.28 ⁇ 0.20°, 21.46 ⁇ 0.20°, 22.74 ⁇ 0.20°, 26.72 ⁇ 0.20°, 27.48 ⁇ 0.20° and 27.82 ⁇ 0.20°.
  • the aforementioned crystal form P has an XRPD pattern as shown in FIG. 59 .
  • the aforementioned crystal form P has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 16D.
  • Table 16D XRPD pattern data for crystal form P No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the present application provides a preparation method for the crystal form P, which comprises: 1) adding a compound of formula (I) to a mixed solvent of MTBE and MeOH; and 2) precipitating a solid and separating to give the crystal form P.
  • the crystal form P is prepared by adding the crystal form A of the compound of formula (I) to the mixed solvent of MTBE and MeOH.
  • the volume ratio of MTBE to MeOH is 3:2.
  • the mass-to-volume ratio of the compound of formula (I) to MTBE and MeOH is selected from 1 mg:0.01-0.4 mL:0.005-0.3 mL, or from 1 mg:0.02-0.1 mL:0.01-0.1 mL, or from 1 mg:0.04 mL:0.027 mL.
  • the present application provides a preparation method for the crystal form P, which comprises: 1) dissolving a compound of formula (I) in methanol or acetone; and 2) precipitating a solid and separating to give the crystal form P.
  • the present application provides a crystal form Q of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.22 ⁇ 0.20° and 14.10 ⁇ 0.20°.
  • the aforementioned crystal form Q has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.22 ⁇ 0.20°, 10.34 ⁇ 0.20°, 14.10 ⁇ 0.20°, 14.66 ⁇ 0.20° and 21.61 ⁇ 0.20°.
  • the aforementioned crystal form Q has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.22 ⁇ 0.20°, 8.53 ⁇ 0.20°, 10.34 ⁇ 0.20°, 14.10 ⁇ 0.20°, 14.66 ⁇ 0.20°, 16.47 ⁇ 0.20°, 17.07 ⁇ 0.20° and 21.61 ⁇ 0.20°.
  • the aforementioned crystal form Q has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.03 ⁇ 0.20°, 8.22 ⁇ 0.20°, 8.53 ⁇ 0.20°, 8.95 ⁇ 0.20°, 10.34 ⁇ 0.20°, 14.10 ⁇ 0.20°, 14.66 ⁇ 0.20°, 15.90 ⁇ 0.20°, 16.47 ⁇ 0.20°, 17.07 ⁇ 0.20°, 19.45 ⁇ 0.20°, 21.61 ⁇ 0.20°, 22.89 ⁇ 0.20° and 23.36 ⁇ 0.20°.
  • the aforementioned crystal form Q has an XRPD pattern as shown in FIG. 47 .
  • the aforementioned crystal form Q has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 17.
  • Table 17. XRPD pattern data for crystal form Q No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.03 100.00 8 15.90 12.63 2 8.22 92.66 9 16.47 11.22 3 8.53 37.31 10 17.07 15.61 4 8.95 12.78 11 19.45 13.79 5 10.34 36.99 12 21.61 19.89 6 14.10 82.75 13 22.89 19.98 7 14.66 39.68 14 23.36 15.53
  • the aforementioned crystal form Q shows a weight loss of 9.29% in a thermogravimetric analysis curve upon heating to 140.0 ⁇ 3 °C.
  • the aforementioned crystal form Q has a TGA pattern as shown in FIG. 48 .
  • the aforementioned crystal form Q has an endothermic peak in a differential scanning calorimetry (DSC) curve at 162.9 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form Q has an endothermic peak in a differential scanning calorimetry (DSC) curve at 235.6 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form Q has an exothermic peak in a differential scanning calorimetry (DSC) curve at 168.5 ⁇ 3 °C.
  • the aforementioned crystal form Q has an endothermic peak in a differential scanning calorimetry (DSC) curve at 162.9 ⁇ 3 °C and/or 235.6 ⁇ 3 °C, and/or has an exothermic peak in the DSC curve at 168.5 ⁇ 3 °C.
  • DSC differential scanning calorimetry
  • the aforementioned crystal form Q has a DSC pattern as shown in FIG. 49 .
  • the aforementioned crystal form Q is a crystal form of a hydrate of the compound of formula (I).
  • a ratio of the number of molecules of the compound of formula (I) to water in the crystal form Q is selected from 1:2.5 to 1:3.5, and preferably 1:3.1.
  • the present application provides a preparation method for the aforementioned crystal form Q, which comprises: 1) dissolving a compound of formula (I) in MeOH, and adding ACN dropwise; and 2) precipitating a solid and separating to give the crystal form Q.
  • the crystal form Q is prepared by adding the crystal form A of the compound of formula (I) to MeOH.
  • the present application provides a crystal form R of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 6.60 ⁇ 0.20°, 8.55 ⁇ 0.20° and 15.21 ⁇ 0.20°.
  • the aforementioned crystal form R has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.60 ⁇ 0.20°, 8.55 ⁇ 0.20°, 11.67 ⁇ 0.20°, 15.21 ⁇ 0.20°, 17.60 ⁇ 0.20° and 24.56 ⁇ 0.20°.
  • the aforementioned crystal form R has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.60 ⁇ 0.20°, 8.55 ⁇ 0.20°, 11.67 ⁇ 0.20°, 15.21 ⁇ 0.20°, 17.12 ⁇ 0.20°, 17.60 ⁇ 0.20°, 2325 ⁇ 0.20°, 24.56 ⁇ 0.20° and 27.31 ⁇ 0.20°.
  • the aforementioned crystal form R has an XRPD pattern as shown in FIG. 50 .
  • the aforementioned crystal form R has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 18.
  • Table 18. XRPD pattern data for crystal form R No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 6.60 63.44 6 17.12 13.85 2 8.55 100.00 7 17.60 21.00 3 11.67 14.28 8 23.25 9.95 4 13.35 4.94 9 24.56 22.29 5 15.21 42.43 10 27.31 16.12
  • the present application provides a preparation method for the aforementioned crystal form R, which comprises: heating the aforementioned crystal form O to 120 °C to 180 °C, and cooling to room temperature to give the crystal form R.
  • the crystal form R is prepared by heating the crystal form O to 150 °C.
  • the present application provides a crystal form S of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 6.15 ⁇ 0.20°, 8.43 ⁇ 0.20°, 21.57 ⁇ 0.20° and 23.90 ⁇ 0.20°.
  • the aforementioned crystal form S has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.15 ⁇ 0.20°, 8.43 ⁇ 0.20°, 14.94 ⁇ 0.20°, 16.29 ⁇ 0.20°, 16.84 ⁇ 0.20°, 21.57 ⁇ 0.20° and 23.90 ⁇ 0.20°.
  • the aforementioned crystal form S has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.15 ⁇ 0.20°, 6.57 ⁇ 0.20°, 8.43 ⁇ 0.20°, 11.27 ⁇ 0.20°, 14.94 ⁇ 0.20°, 16.29 ⁇ 0.20°, 16.84 ⁇ 0.20°, 17.71 ⁇ 0.20°, 21.57 ⁇ 0.20° and 23.90 ⁇ 0.20°.
  • the aforementioned crystal form S has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.15 ⁇ 0.20°, 6.57 ⁇ 0.20°, 8.43 ⁇ 0.20°, 8.83 ⁇ 0.20°, 11.27 ⁇ 0.20°, 13.97 ⁇ 0.20°, 14.23 ⁇ 0.20°, 14.94 ⁇ 0.20°, 16.29 ⁇ 0.20°, 16.84 ⁇ 0.20°, 17.20 ⁇ 0.20°, 17.71 ⁇ 0.20°, 18.48 ⁇ 0.20°, 19.19 ⁇ 0.20°, 20.36 ⁇ 0.20°, 20.74 ⁇ 0.20°, 21.57 ⁇ 0.20°, 22.61 ⁇ 0.20°, 23.02 ⁇ 0.20°, 23.90 ⁇ 0.20°, 26.16 ⁇ 0.20°, 26.67 ⁇ 0.20° and 27.74 ⁇ 0.20°.
  • the aforementioned crystal form S has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.15 ⁇ 0.20°, 6.57 ⁇ 0.20°, 8.43 ⁇ 0.20°, 8.83 ⁇ 0.20°, 9.90 ⁇ 0.20°, 11.27 ⁇ 0.20°, 11.54 ⁇ 0.20°, 13.13 ⁇ 0.20°, 13.97 ⁇ 020°, 14.23 ⁇ 0.20°, 14.94 ⁇ 0.20°, 16.29 ⁇ 0.20°, 16.84 ⁇ 0.20°, 17.20 ⁇ 0.20°, 17.71 ⁇ 0.20°, 18.48 ⁇ 0.20°, 19.19 ⁇ 0.20°, 20.36 ⁇ 0.20°, 20.74 ⁇ 0.20°, 21.57 ⁇ 0.20°, 22.20 ⁇ 0.20°, 22.61 ⁇ 0.20°, 23.02 ⁇ 0.20°, 23.90 ⁇ 0.20°, 24.92 ⁇ 0.20°, 25.58 ⁇ 0.20°, 26.16 ⁇ 0.20°, 26.67 ⁇ 0.20°, 27.74 ⁇ 0.20
  • the aforementioned crystal form S has an XRPD pattern as shown in FIG. 51 .
  • the aforementioned crystal form S has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 19.
  • Table 19 XRPD pattern data for crystal form S No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the present application provides a preparation method for the aforementioned crystal form S, which comprises: heating the aforementioned crystal form E to 180 °C to 240 °C to give the crystal form S.
  • the crystal form S is prepared by heating to 210 °C.
  • the present application provides a crystal form T of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.23 ⁇ 0.20°, 8.45 ⁇ 0.20°, 16.18 ⁇ 0.20° and 26.35 ⁇ 0.20°.
  • the aforementioned crystal form T has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.23 ⁇ 0.20°, 8.45 ⁇ 0.20°, 12.85 ⁇ 0.20°, 16.18 ⁇ 0.20°, 19.41 ⁇ 0.20° and 26.35 ⁇ 0.20°.
  • the aforementioned crystal form T has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.23 ⁇ 0.20°, 8.45 ⁇ 0.20°, 12.85 ⁇ 0.20°, 16.18 ⁇ 0.20°, 18.46 ⁇ 0.20°, 19.41 ⁇ 0.20°, 19.97 ⁇ 0.20°, 21.46 ⁇ 0.20° and 26.35 ⁇ 0.20°.
  • the aforementioned crystal form T has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.23 ⁇ 0.20°, 8.45 ⁇ 0.20°, 9.72 ⁇ 0.20°, 12.85 ⁇ 0.20°, 14.41 ⁇ 0.20°, 16.18 ⁇ 0.20°, 18.46 ⁇ 0.20°, 19.41 ⁇ 0.20°, 19.97 ⁇ 0.20°, 21.46 ⁇ 0.20°, 24.95 ⁇ 0.20° and 26.35 ⁇ 0.20°.
  • the aforementioned crystal form T has an XRPD pattern as shown in FIG. 52 .
  • the aforementioned crystal form T has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 20.
  • Table 20 XRPD pattern data for crystal form T No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) 1 7.23 84.39 7 18.46 17.35 2 8.45 100.00 8 19.41 21.11 3 9.72 6.02 9 19.97 17.27 4 12.85 24.26 10 21.46 24.98 5 14.41 11.88 11 24.95 11.46 6 16.18 26.32 12 26.35 30.07
  • the aforementioned crystal form T shows a weight loss of 0.47% in a thermogravimetric analysis curve upon heating to 150.0 ⁇ 3 °C.
  • the aforementioned crystal form T has a TGA pattern as shown in FIG. 53 .
  • the aforementioned crystal form T has an endothermic peak in a differential scanning calorimetry (DSC) curve at 235.3 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form T has an exothermic peak in a differential scanning calorimetry (DSC) curve at 178.1 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form T has an endothermic peak in a differential scanning calorimetry (DSC) curve at 235.3 ⁇ 3 °C, and/or has an exothermic peak in the DSC curve at 178.1 ⁇ 3 °C.
  • the aforementioned crystal form T has a DSC pattern as shown in FIG. 54 .
  • the present application provides a preparation method for the aforementioned crystal form T, which comprises: heating the aforementioned crystal form G to 120 °C to 180 °C, and cooling to room temperature to give the crystal form T.
  • the crystal form T is prepared by heating the crystal form G to 150 °C.
  • the present application provides a crystal form U of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 3.50 ⁇ 0.20°, 6.97 ⁇ 0.20°, 9.51 ⁇ 0.20° and 19.13 ⁇ 0.20°.
  • the aforementioned crystal form U has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 3.50 ⁇ 0.20°, 6.97 ⁇ 0.20°, 9.51 ⁇ 0.20°, 11.55 ⁇ 0.20°, 17.53 ⁇ 0.20°, 19.13 ⁇ 0.20° and 19.62 ⁇ 0.20°.
  • the aforementioned crystal form U has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 3.50 ⁇ 0.20°, 6.97 ⁇ 0.20°, 9.51 ⁇ 0.20°, 10.29 ⁇ 0.20°, 11.55 ⁇ 0.20°, 14.00 ⁇ 0.20°, 17.53 ⁇ 0.20°, 19.13 ⁇ 0.20°, 19.62 ⁇ 0.20° and 21.09 ⁇ 0.20°.
  • the aforementioned crystal form U has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 3.50 ⁇ 0.20°, 6.97 ⁇ 0.20°, 9.51 ⁇ 0.20°, 9.98 ⁇ 0.20°, 10.29 ⁇ 0.20°, 11.55 ⁇ 0.20°, 14.00 ⁇ 0.20°, 17.53 ⁇ 0.20°, 19.13 ⁇ 0.20°, 19.62 ⁇ 0.20°, 20.71 ⁇ 0.20°, 21.09 ⁇ 0.20°, 21.41 ⁇ 0.20°, 22.32 ⁇ 0.20°, 24.35 ⁇ 0.20°, 26.98 ⁇ 0.20° and 35.53 ⁇ 0.20°.
  • the aforementioned crystal form U has an XRPD pattern as shown in FIG. 55 .
  • the aforementioned crystal form U has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 21.
  • Table 21 XRPD pattern data for crystal form U No. 2 ⁇ ( ⁇ 0.20°) Relative intensity (%) No.
  • the present application provides a preparation method for the aforementioned crystal form U, which comprises: 1) dissolving the compound of formula (I) in DMAc; 2) adding toluene to the resulting DMAc solution; and 3) precipitating a solid and separating to give the crystal form U.
  • the crystal form U is prepared by dissolving the crystal form A of the compound of formula (I) to DMAc.
  • toluene is added to the DMAc solution by evaporating toluene into the DMAc solution.
  • the present application provides a crystal form V of a compound of formula (I) having characteristic diffraction peaks in an X-ray powder diffraction pattern thereof at the following 2 ⁇ : 7.17 ⁇ 0.20°, 9.44 ⁇ 0.20°, 19.06 ⁇ 0.20° and 19.56 ⁇ 0.20°.
  • the aforementioned crystal form V has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 7.17 ⁇ 0.20°, 9.44 ⁇ 0.20°, 10.22 ⁇ 0.20°, 11.48 ⁇ 0.20°, 19.06 ⁇ 0.20°, 19.56 ⁇ 0.20° and 21.35 ⁇ 0.20°.
  • the aforementioned crystal form V has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.90 ⁇ 0.20°, 7.17 ⁇ 0.20°, 8.99 ⁇ 0.20°, 9.44 ⁇ 0.20°, 9.91 ⁇ 0.20°, 10.22 ⁇ 0.20°, 11.48 ⁇ 0.20°, 19.06 ⁇ 0.20°, 19.56 ⁇ 0.20° and 21.35 ⁇ 0.20°.
  • the aforementioned crystal form V has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.90 ⁇ 0.20°, 7.17 ⁇ 0.20°, 8.99 ⁇ 0.20°, 9.44 ⁇ 0.20°, 9.91 ⁇ 0.20°, 10.22 ⁇ 0.20°, 11.48 ⁇ 0.20°, 14.50 ⁇ 0.20°, 17.46 ⁇ 0.20°, 19.06 ⁇ 0.20°, 19.56 ⁇ 0.20°, 21.01 ⁇ 0.20°, 21.35 ⁇ 0.20°, 21.85 ⁇ 0.20°, 22.25 ⁇ 0.20° and 24.27 ⁇ 0.20°.
  • the aforementioned crystal form V has characteristic diffraction peaks in an X-ray powder diffraction pattern at the following 2 ⁇ : 6.90 ⁇ 0.20°, 7.17 ⁇ 0.20°, 8.99 ⁇ 0.20°, 9.44 ⁇ 0.20°, 9.91 ⁇ 0.20°, 10.22 ⁇ 0.20°, 10.41 ⁇ 0.20°, 10.57 ⁇ 0.20°, 11.48 ⁇ 0.20°, 13.93 ⁇ 0.20°, 14.50 ⁇ 0.20°, 17.46 ⁇ 0.20°, 19.06 ⁇ 0.20°, 19.56 ⁇ 0.20°, 20.64 ⁇ 0.20°, 21.01 ⁇ 0.20°, 21.35 ⁇ 0.20°, 21.85 ⁇ 0.20°, 22.25 ⁇ 0.20°, 24.27 ⁇ 0.20°, 26.88 ⁇ 0.20° and 29.30 ⁇ 0.20°.
  • the aforementioned crystal form V has an XRPD pattern as shown in FIG. 56 .
  • the aforementioned crystal form V has characteristic diffraction peaks in an XRPD pattern at the following 2 ⁇ , as shown in Table 22.
  • the aforementioned crystal form V shows a weight loss of 14.05% in a thermogravimetric analysis curve upon heating to 110.0 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form V shows a weight loss of 16.46% in a thermogravimetric analysis (TGA) curve upon heating from 110.0 ⁇ 3 °C to 160.0 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form V shows a weight loss of 14.05% in a thermogravimetric analysis (TGA) curve upon heating to 110.0 ⁇ 3 °C, and/or shows a weight loss of 16.46% in the TGA curve upon heating from 110.0 ⁇ 3 °C to 160.0 ⁇ 3 °C.
  • TGA thermogravimetric analysis
  • the aforementioned crystal form V has a TGA pattern as shown in FIG. 57 .
  • the aforementioned crystal form V has an endothermic peak in a differential scanning calorimetry (DSC) curve at 231.1 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form V has an endothermic peak in a differential scanning calorimetry (DSC) curve at 153.9 ⁇ 3 °C. In some embodiments of the present application, the aforementioned crystal form V has an endothermic peak in a differential scanning calorimetry (DSC) curve at 231.1 ⁇ 3 °C and/or 153.9 ⁇ 3 °C.
  • the aforementioned crystal form V has a DSC pattern as shown in FIG. 58 .
  • the present application provides a preparation method for the aforementioned crystal form V, which comprises: drying the aforementioned crystal form U under vacuum at 50 °C to give the crystal form V.
  • the present application provides a crystal form composition comprising the aforementioned crystal form, wherein the crystal form accounts for 50% or more, preferably 80% or more, more preferably 90% or more and most preferably 95% or more of the weight of the crystal form composition.
  • the present application provides a pharmaceutical composition comprising a therapeutically effective amount of the crystal form or the crystal form composition thereof disclosed herein.
  • the pharmaceutical composition disclosed herein may or may not contain a pharmaceutically acceptable excipient.
  • the pharmaceutical composition disclosed herein may further comprise one or more additional therapeutic agents.
  • the present application also provides use of the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for preparing a medicament for inhibiting nucleoprotein.
  • the present application also provides a method for inhibiting nucleoprotein, which comprises administering to a mammal, preferably a human, in need of such treatment or prevention a therapeutically effective amount of the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof.
  • the present application also provides the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for use as a nucleoprotein inhibitor.
  • the present application also provides use of the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for inhibiting nucleoprotein.
  • the aforementioned use or method is characterized in that the pharmaceutical nucleoprotein inhibitor is a medicament for treating or preventing HBV infection related diseases.
  • the present application also provides use of the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for preparing a medicament for treating or preventing HBV infection related diseases.
  • the present application also provides use of the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for treating or preventing HBV infection related diseases.
  • the present application also provides the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for use in treating or preventing HBV infection related diseases.
  • the present application also provides use of the aforementioned crystal form, the crystal form composition thereof or the pharmaceutical composition thereof for treating or preventing HBV infection related diseases.
  • the compound of formula (I) disclosed herein has good in-vivo drug administration effect, stable crystal forms, small influence of light, heat and humidity, good solubility, and a wide prospect of druggability .
  • the crystal form disclosed herein demonstrates good pharmacokinetics which can be verified by preclinical (e.g., in SD rats and beagle dogs) and clinical trials, and is suitable for use as a medicament.
  • the crystal form disclosed herein contribute to the solid form of the compound.
  • the position and relative intensity of a peak may vary due to measuring instruments, measuring methods/conditions, and other factors.
  • the position of a peak may have an error, and the measurement of 2 ⁇ may have an error of ⁇ 0.2°. Therefore, this error should be considered when determining each crystal form, and crystal forms within this margin of error are within the scope of the present application.
  • preferential orientation The phenomenon that the grains in the sample have a remarkable tendency toward a certain crystallographic direction is called preferential orientation, and the preferential orientation phenomenon can be easily found by visual inspection for a strongly cleaved substance.
  • preferential orientation readily occurs when test samples are made.
  • flaky or needle crystals Like plate crystals, in a cylindrical sample tube, the finding of flaky crystal faces tends to coincide with the axis of the sample tube. In the flat sample holder of the diffractometer, the normal to the flaky crystal face tends to be perpendicular to the basal plane of the sample holder.
  • the diffraction intensity of the preferentially oriented crystal faces is enhanced abnormally when diffraction data are collected using a standard Bragg-Brentano type diffractometer coupled with ⁇ -2 ⁇ . Even though some improvement can be made by making samples many times, it is still difficult to completely overcome the preferential orientation phenomenon ( Measurement of Crystal Structure by Powder Diffraction Method, edited by Liang Jingkui, Science Press, April 2003, 1st editi on).
  • the preferential orientation influences the measurement result of the crystal structure determined by the powder diffraction method.
  • XRPD measurement results of different batches of the crystal form differ, but this does not prevent those skilled in the art from making a decision as to whether the crystal form is the same.
  • the position of an endothermic peak in the DSC pattern may vary due to measuring instruments, measuring methods/conditions, and other factors.
  • there may be an error in the position of the endothermic peak which may be ⁇ 5 °C or may be ⁇ 3 °C. Therefore, this error should be considered when determining each crystal form, and crystal forms within this margin of error are within the scope of the present application.
  • solvate refers to a substance formed by combining the compound of formula (I) with a pharmaceutically acceptable solvent, and water is not included herein.
  • the pharmaceutically acceptable solvent includes ethanol, acetic acid and the like.
  • the solvate includes both stoichiometric and non-stoichiometric amounts of solvates.
  • pharmaceutically acceptable is used herein for those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problems or complications, and commensurate with a reasonable benefit/risk ratio.
  • pharmaceutically acceptable excipient refers to an inert substance administered with active ingredient to facilitate administration of the active ingredient, including, but not limited to, any glidant, sweetener, diluent, preservative, dye/coloring agent, flavor enhancer, surfactant, wetting agent, dispersant, disintegrant, suspending agent, stabilizer, isotonizing agent, solvent or emulsifier acceptable for use in humans or animals (e.g., domesticated animals) as permitted by the National Medical Products Administration, PRC.
  • Non-limiting examples of the excipients include calcium carbonate, calcium phosphate, various sugars and types of starch, cellulose derivatives, gelatin, vegetable oils, and polyethylene glycols.
  • pharmaceutical composition refers to a mixture consisting of one or more of the compounds or the salts thereof of the present application and a pharmaceutically acceptable excipient.
  • the pharmaceutical composition is intended to facilitate the administration of the compound to an organic entity.
  • the pharmaceutical composition of the present application can be prepared by combining the compound of the present application with a suitable pharmaceutically acceptable excipient, and can be formulated, for example, into a solid, semisolid, liquid, or gaseous formulation such as tablet, pill, capsule, powder, granule, ointment, emulsion, suspension, suppository, injection, inhalant, gel, microsphere, and aerosol.
  • a suitable pharmaceutically acceptable excipient such as tablet, pill, capsule, powder, granule, ointment, emulsion, suspension, suppository, injection, inhalant, gel, microsphere, and aerosol.
  • Typical routes of administration of the crystal forms or the pharmaceutical composition thereof disclosed herein include, but are not limited to, oral, rectal, topical, inhalation, parenteral, sublingual, intravaginal, intranasal, intraocular, intraperitoneal, intramuscular, subcutaneous and intravenous administration.
  • the pharmaceutical composition of the present application can be manufactured using methods well known in the art, such as conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, and lyophilizing.
  • the pharmaceutical composition is in an oral form.
  • the pharmaceutical composition can be formulated by mixing the active compounds with pharmaceutically acceptable excipients well known in the art. These excipients enable the compound of the present application to be formulated into tablets, pills, pastilles, dragees, capsules, liquids, gels, slurries, suspensions, etc. for oral administration to a patient.
  • Therapeutic dosages of the compounds disclosed herein may be determined by, for example, the specific use of a treatment, the route of administration of the compound, the health and condition of a patient, and the judgment of a prescribing physician.
  • the proportion or concentration of the compound disclosed herein in a pharmaceutical composition may not be constant and depends on a variety of factors including dosages, chemical properties (e.g., hydrophobicity), and routes of administration.
  • treat or “treatment” means administering the compound or formulation described in the present application to ameliorate or eliminate a disease or one or more symptoms associated with the disease, and includes:
  • prevent means administering the compound or formulation described herein to prevent a disease or one or more symptoms associated with the disease, and includes: preventing the occurrence of the disease or disease state in a mammal, particularly when such a mammal is predisposed to the disease state but has not yet been diagnosed with it.
  • the term "therapeutically effective amount” refers to an amount of a drug or a medicament that is sufficient to provide the desired effect but is non-toxic.
  • the determination of the effective amount varies from person to person. It depends on the age and general condition of a subject, as well as the particular active substance used. The appropriate effective amount in a case may be determined by those skilled in the art in the light of routine tests.
  • the therapeutically effective amount of the crystal forms disclosed herein is from about 0.0001 to 20 mg/kg body weight (bw)/day, for example from 0.001 to 10 mg/kg bw/day.
  • the dosage frequency of the crystal forms disclosed herein depends on needs of an individual patient, e.g., once or twice daily or more times daily. Administration may be intermittent, for example, in a period of several days, the patient receives a daily dose of the crystal forms, and in the following period of several days or more days, the patient does not receive the daily dose of the crystal forms.
  • the intermediate compounds disclosed herein can be prepared by a variety of synthetic methods well known to those skilled in the art, including the specific embodiments listed below, embodiments formed by combinations thereof with other chemical synthetic methods, and equivalents thereof known to those skilled in the art.
  • the preferred embodiments include, but are not limited to, the examples disclosed herein.
  • DCM dichloromethane
  • DMF N,N-dimethylformamide
  • DMSO dimethyl sulfoxide
  • EtOH represents ethanol
  • MeOH represents methanol
  • TFA trifluoroacetic acid
  • ATP represents adenosine triphosphate
  • HEPES represents 4-hydroxyethylpiperazine ethanesulfonic acid
  • EGTA glycol-bis-(2-aminoethylether)tetraacetic acid
  • MgCl 2 represents magnesium dichloride
  • NMP represents N -methylpyrrolidone
  • THF represents tetrahydrofuran
  • 2-MeTHF represents 2-methyltetrahydrofuran
  • MTBE represents methyl tert -butyl ether
  • DMAc represents dimethylacetamide
  • ACN represents acetonitrile.
  • XRPD X-ray powder diffractometer
  • the instrument model is as follows: X'Pert 3 /Empyrean type of X-ray diffractometer from PANalytical.
  • the test method is as follows: approximately 10 mg of the sample was used for XRPD detection.
  • DSC Differential scanning calorimetry
  • the instrument model is as follows: TA Q2000/Discovery DSC 2500 differential scanning calorimeter
  • test method is as follows: a sample (1-5 mg) was placed in a DSC aluminum pan for testing and then heated from 25 °C (room temperature) to a temperature at which the sample would be decomposed at a heating rate of 10 °C/min at 50 mL/min under N 2 atmosphere.
  • TGA Thermal gravimetric analyzer
  • the instrument model is as follows: TA Discovery TGA 5500 thermogravimetric analyzer
  • test method is as follows: a sample (1-5 mg) was placed in a TGA aluminum pan for testing and then heated from room temperature to 350 °C at a heating rate of 10 °C/min at 10 mL/min under N 2 atmosphere.
  • Diffraction intensity data were collected using a Bruker D8 venture diffractometer with Cuk ⁇ radiation as the light source and ⁇ / ⁇ scanning as the scanning mode.
  • Compound 13-6 was separated by SFC (column: DAICELCHIRALCELOJ (250 mm ⁇ 30 mm, 10 ⁇ m); mobile phase: Neu-ETOH; B%: 30%-30%, 9 min) to give compound 1-1 (SFC retention time: 1.7 min), SFC analysis conditions (column: Daicel OJ-3 chiral column, with a specification of 0.46 cm id ⁇ 5 cm; mobile phase: A: carbon dioxide, B: ethanol for chromatography (containing 0.05% isopropylamine); B%: 5%-40%; flow rate: 4 mL/min; 4 min; system back pressure: 100 bar)).
  • the preparation method for the crystal form A was as follows: 7.5 g of compound 1-5 was dissolved in dichloromethane (80 mL), and then trifluoroacetic acid (40 mL) was added. The reaction system was stirred at 15 °C for 1 h. After the reaction was completed as indicated by HPLC, the reaction solution was directly concentrated under reduced pressure. The crude product was purified by slurrying with methyl tert -butyl ether (100 mL), filtered and concentrated, and lyophilized to give the product in the form of a white solid which was separated and subjected to XRPD analysis to give the crystal form A.
  • the preparation method for the crystal form B was as follows: about 15 mg of the crystal form A sample was dissolved in 0.04 mL of DMSO, and water was added dropwise until a solid was precipitated. The solid was suspended and stirred overnight, and then separated and subjected to XRPD analysis to give the crystal form B.
  • the preparation method for the crystal form C was as follows: about 15 mg of the crystal form A sample was dissolved in 0.18 mL of THF, and MTBE was added dropwise until a solid was precipitated. The solid was suspended and stirred overnight, and then separated and subjected to XRPD analysis to give the crystal form C.
  • the preparation method for the crystal form D was as follows: about 15 mg of the crystal form A sample was dissolved in 0.13 mL of THF, and DCM was added dropwise until a solid is precipitated. The solid was suspended and stirred overnight, and then separated and subjected to XRPD analysis to give the crystal form D.
  • the preparation method for the crystal form E was as follows: about 15 mg of the crystal form A sample was dissolved in 0.6 mL of 1,4-dioxane, the above solution was placed in a 3 mL glass bottle, the 3 mL glass bottle containing the above solution was placed in a 20 mL glass bottle containing 3 mL of ACN (acetonitrile) to enable ACN (acetonitrile) to be slowly evaporated into the 1,4-dioxane solution to give a solid in the 1,4-dioxane solution, and the solid was then separated and subjected to XRPD analysis to give the crystal form E.
  • ACN acetonitrile
  • the preparation method for the crystal form F was as follows: about 15 mg of the crystal form A sample was dissolved in 0.3 mL of DMF to give a clear solution which was then added dropwise into 3 mL of H 2 O. The reaction system was suspended and stirred overnight at room temperature, and the solid was separated and subjected to XRPD analysis to give the crystal form F.
  • the preparation method for the crystal form G was as follows: about 15 mg of the crystal form A sample was dispersed in 0.1 mL of CHCl 3 /THF (9:1, v/v), suspended and stirred at room temperature for about 2 weeks, and then separated and subjected to XRPD analysis to give the crystal form G.
  • the preparation method for the crystal form H was as follows: about 15 mg of the crystal form A sample was dispersed in 0.1 mL of EtOH/DMF (19:1, v/v), suspended and stirred at room temperature for about 2 weeks, and then separated and subjected to XRPD analysis to give the crystal form H.
  • the preparation method for the crystal form I was as follows: about 15 mg of the crystal form A sample was dispersed in 0.1 mL of water, suspended and stirred at 50 °C for about 2 weeks, and then separated and subjected to XRPD analysis to give the crystal form I.
  • the preparation method for the crystal form J was as follows: about 15 mg of the crystal form A sample was dispersed in 0.1 mL of 2-MeTHF, suspended and stirred at 50 °C for about 2 weeks, and then separated and subjected to XRPD analysis to give the crystal form J.
  • the preparation method for the crystal form K was as follows: about 15 mg of the crystal form A sample was dissolved in 0.2 mL of DCM/MeOH (4:1, v/v) at 50 °C, directly cooled to 5 °C, and then separated and subjected to XRPD analysis to give the crystal form K.
  • the preparation method for the crystal form L was as follows: about 15 mg of the crystal form A sample was dissolved in 0.1 mL of NMP ( N -methylpyrrolidone), the above solution was placed in a 3 mL glass bottle, the 3 mL glass bottle containing the above solution was placed in a 20 mL glass bottle containing 3 mL of EtOAc (ethyl acetate) to enable EtOAc (ethyl acetate) to be slowly evaporated into the NMP ( N -methylpyrrolidone) solution to give a solid in the NMP ( N -methylpyrrolidone) solution, and the solid was separated and subjected to XRPD analysis to give the crystal form L.
  • NMP N -methylpyrrolidone
  • the preparation method for the crystal form M was as follows: about 15 mg of the crystal form A sample was dissolved in 0.4 mL of THF and slowly evaporated at room temperature to give a solid, and the solid was separated and subjected to XRPD analysis to give the crystal form M.
  • the preparation method for the crystal form N was as follows: about 15 mg of the crystal form A sample was dissolved in 1.5 mL of EtOH at 50 °C, directly cooled to 5 °C, and then separated and subjected to XRPD analysis to give the crystal form N.
  • the preparation method for the crystal form O was as follows: the crystal form D was dried for about 1 h at room temperature under vacuum, and then subjected to XRPD analysis to give the crystal form O.
  • Preparation method 1 for the crystal form P was as follows: about 15 mg of the crystal form A sample was dissolved in 1.0 mL of MTBE/MeOH (3:2, v/v) and slowly evaporated at room temperature to give a solid, and the solid was separated and subjected to XRPD analysis to give the crystal form P.
  • the XRPD measurement results of the resulting crystal form P are shown in FIG. 44A and FIG. 44B , and the TGA and DSC measurement results are shown in FIG. 45 and FIG. 46 , respectively.
  • the preparation method for the crystal form Q was as follows: about 15 mg of the crystal form A sample was dissolved in 1.5 mL of MeOH, about 3 mL of ACN was added dropwise to give a clear solution, and the clear solution was suspended and stirred at -20 °C. The solid was separated and subjected to XRPD analysis to give the crystal form Q.
  • the preparation method for the crystal form R was as follows: the crystal form O was heated to 150 °C, then cooled to room temperature, and then subjected to XRPD analysis to give the crystal form R.
  • the preparation method for the crystal form S was as follows: the crystal form E was heated to 210 °C, and then subjected to in-situ XRPD analysis to give the crystal form S.
  • the preparation method for the crystal form T was as follows: the crystal form G was heated to 150 °C, and then cooled to room temperature to give the crystal form T.
  • the preparation method for the crystal form U was as follows: about 15 mg of the crystal form A sample was dissolved in 0.7 mL of DMAc, toluene was slowly evaporated into the DMAc solution at room temperature to give a clear solution, and the clear solution was evaporated at room temperature, and then separated and subjected to XRPD analysis to give the crystal form U.
  • the preparation method for the crystal form V was as follows: the crystal form U was dried for 2-3 h at 50 °C under vacuum, and then subjected to XRPD analysis to give the crystal form V.
  • Acetone (10.06 L) was added into a reaction kettle, the temperature was controlled at 10-25 °C, and then the crystal form A sample (1342.02 g, 2.49 mol) was added.
  • the reaction system was then stirred at 40 °C for 16-24 h.
  • the reaction was stopped, the reaction solution was directly filtered, and the filter cake was concentrated under reduced pressure at 45 °C to give the compound of formula (I) (1142.51 g, crude).
  • the above procedure was repeated to homogenize the sample twice, the reaction solution was directly filtered, and the filter cake was concentrated under reduced pressure at 45 °C to give the compound of formula (I) (989.01 g, 73.44% yield).
  • the sample was taken and subjected to XRPD analysis, the results are shown in FIG. 59 , and the DSC measurement results are shown in FIG. 60 .
  • the compound of formula (I) was dissolved in methanol and then incubated at room temperature for 10 days by solvent evaporation.
  • the XRPD pattern obtained by calculation through software simulation based on single crystal data is shown in FIG. 61 .
  • the crystal form P was investigated for influence factors (high temperature, high humidity and light), stability under accelerated conditions and stability under intermediate conditions.
  • the crystal form P was placed at high temperature (60 °C, closed), high humidity (room temperature, 92.5% RH, sealing film wrapping and pricking 5-10 small holes) for 5 days and 10 days, then placed under visible light and ultraviolet light (a light-shielding control group was wrapped by tinfoil paper) according to ICH conditions (visible light illumination reached 1.2E+06 Lux hrs, ultraviolet light illumination reached 200 W.hrs/m) in a closed manner, and meanwhile, placed with stability under accelerated conditions (60 °C/75% RH, sealing film wrapping and pricking 5-10 small holes) for 10 days and 1-2 months.
  • HBV DNA content in HepG2.2.15 cells was detected by a real time-qPCR assay, and the inhibitory action of the compound on HBV was evaluated by taking the EC 50 value of the compound as an index.
  • HepG2.2.15 cell culture medium (DMEM/F12, Invitrogen-11330057; 10% serum, Invitrogen-10099141; 100 units/mL penicillin and 10 ⁇ g/mL streptomycin, Invitrogen-15140122; 1% non-essential amino acids, Invitrogen-11140076; 2 mM L-Glutamine, Invitrogen-25030081; 300 ⁇ g/mL geneticin, Invitrogen-10131027)
  • HepG2.2.15 cells (4 ⁇ 10 4 cells/well) were plated in a 96-well plate and cultured overnight at 37 °C and 5 % CO 2 .
  • the sequence of the upstream primer is as follows: GTGTCTGCGGCGTTTTATCA.
  • the sequence of the downstream primer is as follows: GACAAACGGGCAACATACCTT.
  • the sequence of the probe is as follows: 5' + FAM + CCTCTKCATCCTGCTGCTATGCCTCATC + TAMRA -3' 3.6. 15 ⁇ L of the reaction mixture was added into each well of the 96-well PCR plate, and then 10 ⁇ L of sample DNA or HBV DNA standard was added into each well.
  • Reaction conditions for PCR were as follows: heating at 95 °C for 10 min; then denaturating at 95 °C for 15 s and extending at 60 °C for 1 min for 40 cycles.
  • % Inh. [1 - (DNA copy number in the sample - DNA copy number in 1 ⁇ M GLS4)/(DNA copy number in the DMSO control - DNA copy number in 1 ⁇ M GLS4)] ⁇ 100.
  • the cells stably expressing the hERG potassium channel used in the experiment were CHO-hERE from Aviva Biosciences.
  • CHO-hERG was cultured at 37 °C and 5% CO 2 .
  • CHO hERG culture medium is shown in Table 28. Table 28.
  • CHO hERG culture medium Reagent Supplier Volume (mL) F12 culture medium Invitrogen 500 Fetal bovine serum Invitrogen 50 G418/Geneticin Invitrogen 1 Hygromycin B Invitrogen 1
  • the CHO-hERG cells used in the experiment were cultured for at least two days, and the cell density reached 75% or more. Before the experiment, the cells were digested with TrypLE, and then the collected cells were resuspended in extracellular fluid.
  • compositions of the intracellular and extracellular fluids are shown in Table 29. Table 29. Compositions of the intracellular and extracellular fluids Composition Extracellular fluid (mM) Intracellular fluid (mM) NaCl 145 - KCl 4 120 KOH - 31.25 CaCl 2 2 5.374 MgCl 2 1 1.75 Glucose 10 - Na 2 ATP - 4 HEPES 10 10 EGTA - 10 pH pH was adjusted to 7.4 with sodium hydroxide pH was adjusted to 7.4 with potassium hydroxide Osmotic pressure 295mOsm 285mOsm
  • test compound and its positive control amitriptyline were dissolved in DMSO to obtain a stock solution at a certain concentration. Then the stock solution was diluted for different gradients, and finally added to an extracellular fluid at a certain ratio to be diluted to a concentration for test. Precipitation was checked with the naked eye before the experiment. Finally, the concentration of DMSO in the solution to be tested and the positive control amitriptyline should not exceed 0.3%.
  • a voltage stimulation of -50 mv was applied for 80 ms to record the cell leakage current value; then hERG channel was opened by a depolarization to +20 mv for 4800 ms and hERG tail current was elicited by a repolarization to -50 mv for 5000 ms and recorded; and finally, the voltage was restored to the holding potential of-80 mv and maintained for 3100 ms.
  • the above voltage stimulation was repeated every 15000 ms.
  • the hERG QPatch HTX experiment was performed at room temperature. Whole-cell scheme, voltage stimulation scheme and compound detection scheme were established on QPatch Assay Software 5.2 (Sophion Bioscience).
  • C is the tested concentration of the compound, n is the slope, and I is the current.
  • hERG IC 50 values of the compounds in the examples are shown in Table 30. Table 30. hERG IC 50 values of the compounds in the examples Sample hERG IC50 ( ⁇ M) Compound of formula (I) >40
  • test compound (10 mM) was diluted in gradient to prepare working solutions (100 ⁇ final concentration) at concentrations of: 5 mM, 1.5 mM, 0.5 mM, 0.15 mM, 0.05 mM, 0.015 mM and 0.005 mM, and working solutions of positive inhibitors for P450 isoenzymes (CYP1A2, CYP2C9, CYP2C19, CYP2D6 and CYP3A4) and the specific substrate mixtures thereof were prepared simultaneously; human liver microsomes frozen in a -80 °C refrigerator were thawed on ice, and after all thawed, the human liver microsomes were diluted with PB (phosphate buffered saline) to prepare a working solution at a specific concentration (0.253 mg/mL); 20 ⁇ L of the substrate mixture (20 ⁇ L of PB was added into the blank well) and 158 ⁇ L of the working solution of human liver microsomes were added into the reaction
  • PB phosphat
  • the compound was diluted with DMSO (dimethyl sulfoxide) in a 3-fold gradient for 9 concentrations, and added into a 96-well plate in duplicate. The compound concentration was 200-fold of the final test concentration.
  • the cells were rinsed with PBS (phosphate buffered saline) once, added with 0.25% trypsin and digested for about 2-5 min in a 37 °C, 5% CO 2 incubator. Then the digestion was terminated with a cell culture medium and the cells were dispersed into single cells by pipetting with a pipettor. 3. The cell density was counted with a cell counter, and adjusted to the required density with the medium. 4. The cells were added into a 96-well plate that had been added with the compound.
  • the final concentration of DMSO in each well was 0.5%.
  • Wells containing 0.5% DMSO were used as non-toxic negative controls, and wells containing the cell culture medium were used as 100% cytotoxicity controls. Then the cell plate was incubated in a 37 °C, 5% CO 2 cell incubator for 3 days. 5.
  • the chemiluminescence signal (RLU, relative chemiluminescence unit) of each well in the cell plate was detected with the cell viability detection kit CellTiter-Glo using the multi-functional microplate reader Envision, with instructions on the kit followed. 6.
  • test compound (10 mM) was subjected to a two-step dilution, where the compound was diluted to an intermediate concentration of 100 ⁇ M with 100% methanol, and the working solution was diluted to 10 ⁇ M with a potassium phosphate buffer; eight 96-well incubation plates were prepared, and named T0, T5, T10, T20, T30, T60, Blank and NCF60, respectively; the reaction time points corresponding to the first 6 incubation plates were 0 min, 5 min, 10 min, 20 min, 30 min and 60 min, respectively; for the Blank plate, neither the test compound nor a control compound was added, and for the NCF60 plate, potassium phosphate buffer was used in an incubation of 60 min in place of a NADPH regeneration system solution; 10 ⁇ L of the test compound working solution and 80 ⁇ L of the microsome working solution (liver microsome protein concentration was 0.625 mg/mL) were added to the T0, T5, T10, T20, T30, T60
  • test compound (10 mM) was subjected to a two-step dilution, where the compound was diluted to an intermediate concentration of 100 ⁇ M with 100% methanol, and the working solution was diluted to 10 ⁇ M with a potassium phosphate buffer; eight 96-well incubation plates were prepared, and named T0, T5, T10, T20, T30, T60, Blank and NCF60, respectively; the reaction time points corresponding to the first 6 incubation plates were 0 min, 5 min, 10 min, 20 min, 30 min and 60 min, respectively; for the Blank plate, neither the test compound nor a control compound was added, and for the NCF60 plate, potassium phosphate buffer was used in an incubation of 60 min in place of a NADPH regeneration system solution; 10 ⁇ L of the test compound working solution and 80 ⁇ L of the microsome working solution (liver microsome protein concentration was 0.625 mg/mL) were added to the T0, T5, T10, T20, T30, T60
  • test compound was mixed with a solution containing dimethyl sulfoxide (10%), polyethylene glycol 400 (60%) and water (30%), and the mixture was vortexed and sonicated to prepare a 0.2 mg/mL clear solution, which was filtered through a millipore filter for later use.
  • Balb/c female mice aged 7 to 10 weeks were intravenously injected with the candidate compound solution at a dose of 1 mg/kg.
  • test compound was mixed with an aqueous solution containing 10% polyoxyethylene stearate, and the mixture was vortexed and sonicated to prepare a 0.3 mg/mL clear solution for later use.
  • Balb/c female mice aged 7 to 10 weeks were orally administered with the candidate compound solution at a dose of 3 mg/kg.
  • Whole-blood was collected and plasma was prepared.
  • Drug concentration was analyzed by LC-MS/MS and pharmacokinetic parameters were calculated with Phoenix WinNonlin software. The results are shown in Table 35. Table 35.
  • the compound of formula (I) was mixed with an aqueous solution containing 10% polyethylene glycol-15 hydroxystearate, and the mixture was vortexed and sonicated to prepare a 0.3 mg/mL clear solution for later use.
  • Balb/c female mice aged 7 to 10 weeks were orally administered with the candidate compound solution at a dose of 3 mg/kg.
  • the solvent was 10% polyethylene glycol-15 hydroxystearate; a certain amount of the tested compound of formula (I) was dissolved in an aqueous solution containing 10% polyethylene glycol-15 hydroxystearate, and the mixture was vortexed and sonicated to prepare a homogeneous suspension, and the suspension was stored at 4 °C for later use.
  • High pressure injection of the HBV plasmid DNA solution via the tail vein of mice the day of plasmid injection was day 0, the day after injection was day 1, and so on. On day 0, all animals were injected by tail vein with a saline solution containing 10 ⁇ g of plasmid DNA at a volume of 8% of body weight, and the injection was completed within 5 seconds.
  • mice were administered intragastrically twice a day (8/16 h interval) on day 1-6 and once on day 7. All mice were euthanized in the afternoon on day 7. The body weight of the mice, which was monitored every day, remained stable throughout the experiment.
  • Sample collection blood was collected from the submandibular vein 4 h after the first administration in the morning on days 1, 3, and 5. All blood samples were collected in K 2 -EDTA anticoagulation tubes, and centrifuged for 10 min at 4 °C, 7000 g to prepare about 40 ⁇ L of plasma. All mice were euthanized by CO 2 four hours after administration in the morning on day 7. Blood was collected from the heart, and the plasma preparation method was the same as above. Two liver tissues were collected with 70-100 mg each, and quick-frozen by liquid nitrogen. After all samples were collected, they were stored in a refrigerator (-80 °C) for HBV DNA content detection.

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
EP20890696.6A 2019-11-22 2020-11-20 Kristallform des nukleoproteininhibitors und verwendung davon Withdrawn EP4063366A4 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201911171978 2019-11-22
PCT/CN2020/130612 WO2021098850A1 (zh) 2019-11-22 2020-11-20 一种核蛋白抑制剂的晶型及其应用

Publications (2)

Publication Number Publication Date
EP4063366A1 true EP4063366A1 (de) 2022-09-28
EP4063366A4 EP4063366A4 (de) 2023-12-20

Family

ID=75980397

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20890696.6A Withdrawn EP4063366A4 (de) 2019-11-22 2020-11-20 Kristallform des nukleoproteininhibitors und verwendung davon

Country Status (7)

Country Link
US (1) US20230026869A1 (de)
EP (1) EP4063366A4 (de)
JP (1) JP2023502675A (de)
CN (1) CN114728973A (de)
AU (1) AU2020385518A1 (de)
CA (1) CA3159096A1 (de)
WO (1) WO2021098850A1 (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11247965B2 (en) 2017-12-11 2022-02-15 VenatoRx Pharmaceuticals, Inc. Hepatitis B capsid assembly modulators
GB2583614B (en) 2018-06-11 2023-05-24 Venatorx Pharmaceuticals Inc Hepatitis B capsid assembly modulators

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2159224T3 (pl) 2007-06-18 2012-12-31 Ruyuan Wei Xiang Tech Co Ltd Tiazolilohydropirymidyny podstawione bromofenylem
TWI730985B (zh) * 2015-09-15 2021-06-21 美商艾森伯利生物科學公司 B型肝炎核心蛋白質調節劑
CA3017020C (en) * 2016-03-07 2024-01-16 Enanta Pharmaceuticals, Inc. Hepatitis b antiviral agents
JOP20190024A1 (ar) * 2016-08-26 2019-02-19 Gilead Sciences Inc مركبات بيروليزين بها استبدال واستخداماتها
CN107778310A (zh) * 2016-08-31 2018-03-09 上海市第人民医院 乙肝病毒靶向人La蛋白的抑制剂HBSC11及其衍生物和用途
EP3759109B1 (de) * 2018-02-26 2023-08-30 Gilead Sciences, Inc. Substituierte pyrrolizinverbindungen als hbv-replikationsinhibitoren
CN113549079A (zh) * 2018-05-25 2021-10-26 正大天晴药业集团股份有限公司 2,3-二氢-1h-吡咯嗪-7-甲酰胺类衍生物及其应用

Also Published As

Publication number Publication date
JP2023502675A (ja) 2023-01-25
CA3159096A1 (en) 2021-05-27
EP4063366A4 (de) 2023-12-20
AU2020385518A1 (en) 2022-06-09
WO2021098850A1 (zh) 2021-05-27
CN114728973A (zh) 2022-07-08
US20230026869A1 (en) 2023-01-26

Similar Documents

Publication Publication Date Title
CN110577536B (zh) 苯甲酰氨基吡啶衍生物的盐及其在药物中的应用
US10301287B2 (en) Solid forms of cenicriviroc mesylate and processes of making solid forms of cenicriviroc mesylate
EP4063366A1 (de) Kristallform des nukleoproteininhibitors und verwendung davon
KR20140138941A (ko) 상피 성장 인자 수용체 키나제 억제제의 염
CN110577533A (zh) 苯甲酰氨基吡啶衍生物的盐及其在药物中的应用
EP4036078A1 (de) Kristalline form eines kapsidproteinassemblierungsinhibitors mit einem heterofünfgliedrigen ring und verwendung davon
JP2020502129A (ja) Ｎｒｆ２アクチベーターとしての３−オキソ−１，４−ジアゼピニル化合物
WO2021143843A1 (zh) 一种pde3/pde4双重抑制剂的结晶及其应用
JP2022504765A (ja) ジヒドロイミダゾピラジノン化合物、該化合物を含む組成物およびその使用
US20220332684A1 (en) Crystal form of five-membered n heterocyclic compound, and application thereof
WO2018041260A1 (zh) 一类溴结构域识别蛋白抑制剂及其制备方法和用途
WO2021129841A1 (zh) 用作ret激酶抑制剂的化合物及其应用
CN111094241B (zh) 一种氧代吡啶酰胺类衍生物的晶型及其制备方法
CN117797146A (zh) Sarm1酶活性抑制剂及其在神经退行性疾病中的应用
TW202337444A (zh) 解旋酶引子酶抑制劑的固體結晶形式及其製備方法
EP3560944A1 (de) Feste form einer 4'-thio-2'-fluornukleosid-phosphamid-verbindung und herstellungsverfahren dafür und verwendung davon
US20220162185A1 (en) Crystalline and amorphous forms of n-(5-((4-ethylpiperazin-1-yl)methyl)pyridine-2-yl)-5-fluoro-4-(3-isopropyl-2-methyl-2h-indazol-5-yl)pyrimidin-2-amine and its salts, and preparation methods and therapeutic uses thereof
EP3696166B1 (de) Amorphes pyrrolidinderivat als ppar-agonist und herstellungsverfahren dafür
KR102397741B1 (ko) 세고리식 화합물의 결정 형태 및 이의 용도
EP3978476A1 (de) Feste form einer aromatischen verbindung und verfahren zu ihrer herstellung
WO2019149090A1 (zh) 一种尿酸转运体1抑制剂的晶体及其制备方法和用途
WO2022262841A1 (zh) 一种螺环化合物的盐型、晶型及其制备方法
EP4194455A1 (de) Kristallformen von pyridopyrazolverbindungen und herstellungsverfahren dafür
WO2019086008A1 (zh) 一种苯并三氮唑衍生物的晶型及其制备方法和用途
KR102660247B1 (ko) 4-(나프탈렌-1-일)-4h-1, 2, 4-트리아졸계 화합물의 결정 형태, 염 형태 및 이의 제조방법

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20220621

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN

A4 Supplementary search report drawn up and despatched

Effective date: 20231116

RIC1 Information provided on ipc code assigned before grant

Ipc: A61P 31/12 20060101ALI20231110BHEP

Ipc: A61K 31/407 20060101ALI20231110BHEP

Ipc: C07D 487/04 20060101AFI20231110BHEP

18W Application withdrawn

Effective date: 20231122